Medtronic shares slip on missed Q2 sales mark, lowered outlook

BY

Medtronic (NYSE:MDT) shares dropped in pre-market trading today after the world’s largest medical device company missed Wall Street’s expectations with its fiscal 2nd-quarter sales and lowered its outlook for the rest of the year.

Fridley, Minn.-based Medtronic posted profits of $1.12 billion, or 80¢ per share, on sales of $7.35 billion for the 3 months ended Oct. 28, for bottom-line growth of 114.4% on sales growth of 4.1% compared with Q2 2015.

Adjusted to exclude 1-time items, earnings per share were $1.18, 6¢ ahead of the forecast on The Street. But analysts there were looking for sales of $7.46 billion; investors reacted by pushing MDT shares down -7.3% to $74.70 in pre-market activity today.

“Q2 revenue was disappointing and did not meet our expectations. We faced issues that affected our growth, including slower-than-expected revenue as we await new product introductions, particularly in CVG and Diabetes,” chairman & CEO Omar Ishrak said in prepared remarks. “Despite this revenue shortfall, we produced a strong improvement in operating margins and double digit constant currency earnings per share growth.”

 

READ THE REST HERE

First Choice Healthcare Solutions Issues Formal Financial Guidance for 2017 Full Year Revenues and Adjusted EBITDA Margin

MELBOURNE, FL–(Marketwired – Nov 22, 2016) – First Choice Healthcare Solutions, Inc.(OTCQB: FCHS) (“FCHS,” “First Choice” or the “Company”), one of the nation’s only non-physician-owned, publicly traded healthcare services companies focused on the delivery of total musculoskeletal solutions with an emphasis on Orthopaedics, including spine care and treatment, today issued formal financial guidance of $40-$45 million for 2017 full year revenues and 15%-20% for 2017 full year adjusted EBITDA margin.

Company President and CEO Chris Romandetti, noted, “As discussed on our recent third quarter results conference call, we are very confident in First Choice’s ability to perpetuate our success with executing key organic and strategic initiatives designed to fuel our revenue and earnings growth through 2017. More specifically, organic growth will stem from the following:

  • the addition of new surgeons and physician assistants who have signed to join our clinical teams between now and the first quarter of next year;
  • increasing the number of Orthopaedic and Spine surgical procedures we perform each year due to the aforementioned expansion of our medical team — in 2016, we saw this number grow from an annualized run-rate of approximately 2400+ in Q116 to 3100+ in Q316, and expect to increase it to 5,000 in 2017;
  • expansion of our Physical and Occupational Therapy division throughout the greater Space Coast, Florida service region; and
  • materially increasing utilization of our ambulatory surgery center facilities and services.

“First Choice’s strategic growth will be propelled by possible acquisition of other healthcare service businesses that will either enhance or expand our current ancillary service lines and through the launch of our Orthopaedic bundled payment pilot programs early in the new year,” Romandetti added. “Given our confidence in successfully executing these, among other initiatives, we have no reservations about issuing formal revenue guidance of $40-$45 million for next year and adjusted EBITDA guidance of 15-20%. However, as we move through the new year, we will reevaluate our guidance quarterly and revise or reiterate our expectations, as appropriate.”

For those unable to participate on First Choice’s live third quarter results conference call, an audio replay of the event is available on the Company’s website investor relations page, found at http://ir.myfchs.com/.

About First Choice Healthcare Solutions, Inc.
Headquartered in Melbourne, Florida, First Choice Healthcare Solutions (FCHS) is implementing a defined growth strategy aimed at expanding its network of non-physician-owned medical centers of excellence, which concentrate on treating patients in the following specialties: Orthopaedics, Spine Surgery, Neurology, Interventional Pain Management and related diagnostic and ancillary services in key expansion markets throughout the Southeastern U.S. Serving Florida’s Space Coast, the Company’s flagship integrated platform currently administers over 100,000 patient visits each year and is comprised of First Choice Medical Group, The B.A.C.K. Center and Crane Creek Surgery Center. For more information, please visit www.myfchs.com, www.myfcmg.com, www.thebackcenter.net and www.cranecreeksurgerycenter.com.

Safe Harbor Statement
Certain information set forth in this news announcement may contain forward-looking statements that involve substantial known and unknown risks and uncertainties. These forward-looking statements are subject to numerous risks and uncertainties, certain of which are beyond the control of First Choice Healthcare Solutions, Inc. Such forward-looking statements are based on current expectations, estimates and projections about the Company’s industry, management beliefs and certain assumptions made by its management. Readers are cautioned that the assumptions used in the preparation of such information, although considered reasonable at the time of preparation, may prove to be imprecise and, as such, undue reliance should not be placed on forward-looking statements. Information concerning factors that could cause the Company’s actual results to differ materially from those contained in these forward-looking statements can be found in the Company’s periodic reports on Form 10-K and Form 10-Q, and in its Current Reports on Form 8-K, filed with the Securities and Exchange Commission. Unless required by law, the Company undertakes no obligation to update publicly any forward-looking statements, whether as a result of new information, future events, or otherwise to reflect future events or circumstances or reflect the occurrence of unanticipated events.

CONTACT INFORMATION

Konica Minolta Partners with Mindray to Further Expand MSK Ultrasound Portfolio

WAYNE, NJ –(Marketwired – November 21, 2016) – Konica Minolta Healthcare announced today it has entered into a partnership with Mindray, a leading developer, manufacturer and marketer of medical devices worldwide, to bring exclusive musculoskeletal (MSK) portable ultrasound solutions to the market. Konica Minolta solidifies its leadership position in MSK imaging by continuing to establish partnerships and develop solutions that enable specialists to deliver the best care possible to their patients.

“The unique relationship with Mindray further underscores Konica Minolta’s commitment to being a market leader in MSK ultrasound,” said Brian Noyes, Sr. Vice President and General Manager, Ultrasound Division. “Mindray’s dedication to improving patient care complements Konica Minolta’s cutting-edge technologies and award-winning customer satisfaction.”

Konica Minolta is committed to providing physicians with solutions that assist with more accurate assessment and treatments of musculoskeletal ailments. “It’s important to place excellent technology in the hands of MSK experts who can support orthopedists, sports medicine physicians, rheumatologists, podiatrists and beyond,” said Glen McLaughlin, Chief Product Officer of Mindray Ultrasound. “Konica Minolta has extensive experience in this field and is a longstanding provider of MSK solutions to this group of specialists.”

The partnership with Mindray addresses the need for cutting-edge ultrasound technology in out-of-hospital settings like MSK, and demonstrates Konica Minolta’s commitment to develop strategic relationships, Noyes explained.

“By working together, industry experts bring value to musculoskeletal providers by giving them the best tools at the point of care,” he added.

About Konica Minolta Healthcare Americas, Inc.
Konica Minolta Healthcare Americas, Inc. is a world-class provider and market leader in medical diagnostic imaging and healthcare information technology. With over 75 years of endless innovation, Konica Minolta is globally recognized as a leader providing cutting-edge technologies and comprehensive support aimed at providing real solutions to meet customer’s needs. Konica Minolta Healthcare Americas, Inc., headquartered in Wayne, NJ, is a unit of Konica Minolta, Inc. (TSE: 4902). For more information on Konica Minolta Healthcare Americas, Inc., please visit www.konicaminolta.com/medicalusa.

Company name KONICA MINOLTA, INC.
Headquarters JP TOWER, 2-7-2 Marunouchi, Chiyoda-ku, Tokyo, Japan
Founded December 1936
FY 2015 Revenue $8.6 Billion
Number of employees Approx. 41,600 (2015)
Business Lines The Konica Minolta Group operates in sectors ranging from business technologies, where our products are typified by MFPs (multi-functional peripherals), and Industrial Business (former Optics Business), where our products include pickup lenses for optical disks, and TAC film, a key material used in LCD panels, to healthcare, where we make digital X-ray diagnostic imaging systems.

CONTACT INFORMATION

SPINEWAY : Increase in capital of €1.4 million and entry of TINAVI Medical Technologies into Spineway”s capital

By GlobeNewswire,  November 21, 2016

SPINEWAY, a company specialising in implants and surgical instruments for the treatment of vertebral (spinal) problems, is proud to announce that the Chinese company TINAVI Medical Technologies has joined its capital, following a €1.4 million increase in capital.

Following approval by the General Meeting on 4 November, Spineway increased its reserve capital through the issue of shares with attached warrants (Actions à Bons de Souscription d’Actions or ABSA in French) excluding preferential right of subscription, for a total of €1.4 million (including issue premium).

This increase in capital, made on November 18 through the issue of 355,260 new shares with attached warrants, was paid for entirely by TINAVI Medical Technologies, which now holds 9.09% of the capital and 5.04% of Spineway’s voting rights.

Stéphane Le Roux, Chief Executive Officer of Spineway, says: “We are delighted to welcome TINAVI Medical Technologies into our capital. In keeping with our Skyway 2018 plan, this partnership will open great potential for our development in China, which is a key nation in our Group’s history. On top of that, the synergies between our areas of expertise and know-how will help our respective companies grow and develop more rapidly in the spinal surgery market, which is continually striving to innovate.”

Find out all about Spineway at www.spineway.com

SPINEWAY IS ELIGIBLE FOR THE PEA-PME (EQUITY SAVINGS PLAN FOR SMES)

Spineway designs, manufactures and markets innovative implants and surgical instruments for treating severe disorders of the spinal column.

Spineway has an international network of over 50 independent distributors and 90% of its turnover comes from exports.

Spineway, which is eligible for investment through FCPIs (French unit trusts specializing in innovation), received the OSEO Excellence award as well as the Deloitte Fast 50 award in 2011. Rhône Alpes INPI Patent Innovation Award (2013) -Talent INPI award (2015).

Contacts:

Investor Relations

David Siegrist, Finance Director

Tel: +33 (0)4 72 77 01 52

finance.dsg@spineway.com

Financial Communication

Jérôme Gacoin / Solène Kennis

Tel: +33 (0)1 75 77 54 68

skennis@aelium.fr

Capital increase and Tinavi entry

This announcement is distributed by Nasdaq Corporate Solutions on behalf of Nasdaq Corporate Solutions clients.

The issuer of this announcement warrants that they are solely responsible for the content, accuracy and originality of the information contained therein.

Source: SPINEWAY via Globenewswire

 

This article appears in: News Headlines

Referenced Stocks: ALSPW

Read more: http://www.nasdaq.com/press-release/spineway–increase-in-capital-of-14-million-and-entry-of-tinavi-medical-technologies-into-spineway-20161121-00727#ixzz4QqLO33ND

Zimmer Biomet Named Indo UK Institutes of Health Medicities Program’s Preferred Orthopaedic Partner to Improve Delivery of Care in India

WARSAW, Ind., Nov. 22, 2016 /PRNewswire/ — Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH), a global leader in musculoskeletal healthcare, today announced that the Company has been chosen as an Indo UK Institutes of Health (IUIH) preferred orthopaedic partner to improve the delivery of and access to quality, affordable musculoskeletal healthcare for approximately 400 million people in India over the next 20 years through IUIH’s 11 centers of excellence (“Medicities”) to be created in major states across the country.  IUIH Medicities will offer patients throughout India and abroad access to world-class services and clinical expertise in a modern, technology-led hospital.  In addition, each Medicity will establish a medical college, nursing college, post-graduate training center, global standard research and development center and medical manufacturing facilities.  The partnership was announced by the IUIH Medicities Program at the India-UK Technology Summit inaugurated by the Prime Minister of India, Narendra Modi, and the Prime Minister of the UK, Theresa May.  The UK Secretary of State for International Trade, Dr. Liam Fox, chaired the roundtable that announced the partnership.

“At its one-year anniversary, the IUIH Medicities Program is delighted to announce Zimmer Biomet as a preferred orthopaedic partner for the next two decades,” said Ajay Rajan Gupta, M.D., Group Chief Executive Officer of IUIH.  “IUIH shares Zimmer Biomet’s commitment to improve the quality of life for patients around the world.  This partnership demonstrates a significant step toward achieving our vision to transform the delivery of quality healthcare and medical education services across India.”

The newly created partnership between IUIH and Zimmer Biomet delivers value throughout the orthopaedic care continuum.  Total Zimmer Biomet commitments to the program include an equity investment in UK Global Healthcare Limited (UKGH), the parent organization for IUIH; the supply and distribution of quality large joint implants, trauma products and small fixation devices for replacement surgery; the implementation of the Rapid Recovery and Theatre Care Rapide programs to optimize patient-focused processes and protocols in the hospitals and operating rooms across the 11 Medicities; and the establishment of the Zimmer Biomet Institute of India, a state-of-the-art medical training and education facility.  In addition to the opportunity to improve patient outcomes, the efficiencies created through the long-term partnership are expected to significantly contribute to the delivery of affordable care in India by reducing the total cost of orthopaedic care by approximately 25 percent.

“Zimmer Biomet is proud to be chosen as a preferred orthopaedic partner for the IUIH Medicities program,” said David Dvorak, President and CEO of Zimmer Biomet.  “This long-term commitment demonstrates an unprecedented level of partnership between a forward-looking healthcare provider and a leading musculoskeletal healthcare company, putting transformational patient care and exponential value creation within reach.”

About Zimmer Biomet

Founded in 1927 and headquartered in Warsaw, Indiana, Zimmer Biomet is a global leader in musculoskeletal healthcare. We design, manufacture and market orthopaedic reconstructive products; sports medicine, biologics, extremities and trauma products; office based technologies; spine, craniomaxillofacial and thoracic products; dental implants; and related surgical products.

We collaborate with healthcare professionals around the globe to advance the pace of innovation. Our products and solutions help treat patients suffering from disorders of, or injuries to, bones, joints or supporting soft tissues. Together with healthcare professionals, we help millions of people live better lives.

We have operations in more than 25 countries around the world and sell products in more than 100 countries. For more information, visit www.zimmerbiomet.com or follow Zimmer Biomet on Twitter at www.twitter.com/zimmerbiomet.

About Indo UK Institutes of Health

On November 12, 2015, the Indian and British Prime Ministers signed a historic Health Collaboration Agreement for the establishment of the Indo UK Institutes of Health (IUIH). The IUIH is a Private Public Partnership (Indo UKpartnership) that is linked to the Indian Government’s Smart Cities programme and aims to build 11 IUIH “Medicities” along with 89 Indo UK Clinics (IUCs).

The IUIH facilities’ global operations and research expertise will be supported by collaboration with the UK National Health Service (NHS) and partnerships with leading international healthcare industry companies and international partners in research, education, manufacturing and healthcare delivery.

The vision is to develop fully integrated healthcare that is Affordable, Available and Accountable.

Please visit iuih.co.uk for more information or contact victoria.lusher@iuih.co.uk.

Cautionary Statement Regarding Forward-Looking Statements

This news release contains forward-looking statements within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.  Forward-looking statements include, but are not limited to, statements concerning Zimmer Biomet’s expectations, plans, prospects, and product and service offerings, including new product launches and potential clinical successes.  Such statements are based upon the current beliefs and expectations of management and are subject to significant risks and uncertainties that could cause actual outcomes and results to differ materially.  For a list and description of some of such risks and uncertainties, see our periodic reports filed with the SEC.  These factors should not be construed as exhaustive and should be read in conjunction with the other cautionary statements that are included in Zimmer Biomet’s filings with the SEC.  We disclaim any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as may be set forth in our periodic reports.  Accordingly, such forward-looking statements speak only as of the date made.  Readers of this news release are cautioned not to place undue reliance on these forward-looking statements, since, while management believes the assumptions on which the forward-looking statements are based are reasonable, there can be no assurance that these forward-looking statements will prove to be accurate.  This cautionary statement is applicable to all forward-looking statements contained in this news release.

Logo – http://photos.prnewswire.com/prnh/20150624/225371LOGO

To view the original version on PR Newswire, visit:http://www.prnewswire.com/news-releases/zimmer-biomet-named-indo-uk-institutes-of-health-medicities-programs-preferred-orthopaedic-partner-to-improve-delivery-of-care-in-india-300367537.html

SOURCE Zimmer Biomet Holdings, Inc.

News Provided by Acquire Media

Global Surgical Navigation Systems Market to Witness Growth Through 2020, Owing to Popularity of Minimally Invasive Surgeries: Reports Technavio

November 22, 2016

LONDON–(BUSINESS WIRE)–Technavio analysts forecast the global surgical navigation systems market to grow at a CAGR of more than 7% during the forecast period, according to their latest report.

The research study covers the present scenario and growth prospects of the global surgical navigation systems market for 2016-2020. The report segments the market by application into neurosurgical, spine, orthopedic, and ENT surgical navigation systems.

According to Barath Palada, a lead analyst at Technavio for medical devicesresearch, “The launch of portable surgical navigation systems is a new trend in the market which can help solve the issue of space constraints in the already crowded hybrid operating rooms and can also be moved to low-tier hospitals on a fee-per-use basis for critical surgeries.”

Request a sample report: http://www.technavio.com/request-a-sample?report=54564

Technavio’s sample reports are free of charge and contain multiple sections of the report including the market size and forecast, drivers, challenges, trends, and more.

Technavio healthcare and life sciences analysts highlight the following three factors that are contributing to the growth of the global surgical navigation systems market:

  • Growing popularity of minimally invasive surgeries
  • Expansion of outpatient settings
  • Innovative marketing strategies

Growing popularity of minimally invasive surgeries

The growing incidence of complications for open surgeries and slow post-operative healing of the incision area has led to a rise in adoption of minimally invasive techniques for surgery. Surgical navigation systems with advanced intraoperative imaging system and wide high-resolution monitors enable surgeons to perform even critical surgeries with minimal incision of skin.

Growing demand for minimally invasive surgeries coupled with the awareness related to its benefits has led a large section of surgeons to opt for computer-assisted surgery using surgical navigation systems.

Expansion of outpatient settings

Many surgeons have started practicing surgeries using surgical navigation systems in an outpatient setting, especially for spinal, ENT, and orthopedic disorders. This trend is expected to continue, and very soon many complicated open surgeries will undergo a rapid transition into minimally invasive surgeries performed with surgical navigation systems. “The procedures performed by surgical navigation systems reduce the risk of hospital-acquired infections and hospital stay, cause minimal blood loss, scarring, and less pain, thus leading to a quick recovery and better clinical outcome,” says Barath.

Thus, there is an opportunity for surgeons to invest in setting up ambulatory surgery centers (ASCs) to perform various spinal, ENT, and orthopedic surgeries in an outpatient setting. Low-priced ENT-specific navigation platforms represent a cost-effective option for surgeons performing outpatient procedures.

Innovative marketing strategies

Surgical navigation system vendors are implementing innovative marketing strategies such as offering cumulative training/medical education classes to surgeons and other healthcare professionals, to increase awareness and adoption of these systems and thereby leading to an increase in the sales of products. For instance, Medtronic offers educational programs for orthopedic, spinal, and ENT procedures.

OrthAlign recently launched OrthAlign Academy, an online portal dedicated to educating surgeons and hospital staff on the use of its KneeAlign technology for total knee arthroplasty surgery. KneeAlign offers tibial and femoral navigation in a simple, palm-sized, single-use device and is compatible with all implant systems. Other strategies include offering fee-per-use of equipment, customer portals, and operating room assistance facilities to end-users.

The US, Western Europe, and Japan are the primary markets for these vendors, whereas emerging markets such as India, Brazil, China, and Mexico serve as opportunities for increased penetration and revenue generation during the forecast period.

Browse Related Reports:

Do you need a report on a market in a specific geographical cluster or country but can’t find what you’re looking for? Don’t worry, Technavio also takes client requests. Please contact enquiry@technavio.com with your requirements and our analysts will be happy to create a customized report just for you.

About Technavio

Technavio is a leading global technology research and advisory company. The company develops over 2000 pieces of research every year, covering more than 500 technologies across 80 countries. Technavio has about 300 analysts globally who specialize in customized consulting and business research assignments across the latest leading edge technologies.

Technavio analysts employ primary as well as secondary research techniques to ascertain the size and vendor landscape in a range of markets. Analysts obtain information using a combination of bottom-up and top-down approaches, besides using in-house market modeling tools and proprietary databases. They corroborate this data with the data obtained from various market participants and stakeholders across the value chain, including vendors, service providers, distributors, re-sellers, and end-users.

If you are interested in more information, please contact our media team at media@technavio.com.

Contacts

Technavio Research
Jesse Maida
Media & Marketing Executive
US: +1 630 333 9501
UK: +44 208 123 1770
www.technavio.com

Amedica Slides on Mixed FDA Updates

 November 22, 2016

Amedica Corp. (NASDAQ: AMDA) is watching its shares drop on Tuesday despite receiving mixed news from the U.S. Food and Drug Administration, along with a new appointment to its management team. Although the FDA did give some good news, the bad far outweighed the good.

First the company announced that Dana Lyons has been appointed to Vice President of Sales and Marketing, in an effort to increase the adoption of silicon nitride implants in the spinal fusion market. Previously, Lyons has worked in leadership positions with Stryker Orthopaedics, Zimmer Spine, and Zimmer Biomet Spine.

As for the good news, the FDA also notified Amedica that the new pedicle screw system, Taurus, has been cleared for commercialization. The company is on target for surgical implantation and a full market launch of the Taurus system by the end of the year.

B. Sonny Bal, MD, MBA, JD, PhD; the CEO and President of Amedica Corporation commented:

Amedica is building a top-tier sales team with skilled veterans from the spine industry, such as Mr. Lyons. Going forward, our focus is on driving sales, surgeon engagement, and data collection to validate the unparalleled volume of basic material science data that we have already published. Surgeon intrigue about our material, and a market need for clinical advantages that only our material can deliver, combine to make spine an attractive growth opportunity. As part of the new sales team, I will focus on driving clinical trials, surgeon relations, and publishing clinical data to impact our revenue growth.

 

READ THE REST HERE

Zimmer Biomet Announces Cash Tender Offers for Up to $1.1 Billion Aggregate Purchase Price of Certain Outstanding Debt Securities

WARSAW, Ind., Nov. 21, 2016 /PRNewswire/ — Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH) (the “Company”) today announced the commencement of cash tender offers (collectively, the “Offers”) for up to $1.1 billion aggregate purchase price (excluding accrued and unpaid interest to, but not including, the applicable settlement date and excluding fees and expenses related to the Offers) (the “Maximum Tender Amount”) of its 5.750% Senior Notes due 2039, its 4.450% Senior Notes due 2045, its 4.250% Senior Notes due 2035, its 3.550% Senior Notes due 2025 and its 4.625% Senior Notes due 2019 (collectively, the “Notes”). The purpose of the Offers is to reduce the principal amount of the Company’s outstanding debt securities. Notes purchased in the Offers will be retired and cancelled.

The following table sets forth certain information regarding the Notes and the Offers:

Title of Security

CUSIP
Number

Principal
Amount
Outstanding

Tender Cap(1)

Acceptance
Priority
Level

Reference U.S.
Treasury
Security

Bloomberg
Reference
Page(2)

Fixed Spread
(basis
points)

Early
Tender
Premium
(per $1,000)

Hypothetical Total Consideration (per $1,000)(3)

5.750% Senior Notes due 2039

98956PAB8

$   500,000,000

$250,000,000

1

2.25% UST due 8/15/2046

FIT1

170

$30.00

$1,140.39

4.450% Senior Notes due 2045

98956PAH5

$1,250,000,000

N/A

2

2.25% UST due 8/15/2046

FIT1

170

$30.00

$   954.73

4.250% Senior Notes due 2035

98956PAG7

$   500,000,000

N/A

3

2.25% UST due 8/15/2046

FIT1

155

$30.00

$   957.62

3.550% Senior Notes due 2025

98956PAF9

$2,000,000,000

$200,000,000

4

2.00% UST due 11/15/2026

FIT1

130

$30.00

$   994.70

4.625% Senior Notes due 2019

98956PAA0

$   500,000,000

$200,000,000

5

1.00% UST due 11/15/2019

FIT1

65

$30.00

$1,075.53

(1) The Tender Cap for each series represents the maximum aggregate principal amount of Notes of such series that will be purchased in the Offers.

(2) The applicable page on Bloomberg from which the dealer managers will quote the bid side prices of the applicable U.S. Treasury Security. In the above table, “UST” denotes a U.S. Treasury Security.

(3) The Hypothetical Total Consideration is inclusive of the Early Tender Premium (as defined below) but exclusive of accrued and unpaid interest from the last interest payment date applicable to the relevant series of Notes up to, but not including, the Early Settlement Date (as defined below) and is based on the reference yield of the Reference U.S. Treasury Security as of 11:00 a.m., New York City time, on November 18, 2016. The actual reference yields of the Reference U.S. Treasury Securities will be determined by the dealer managers based on certain quotes available at 11:00 a.m., New York City time, on the price determination date, which is expected to be December 6, 2016.

The Offers are being made pursuant to and are subject to the terms and conditions, including a financing condition, set forth in the Offer to Purchase dated November 21, 2016 (the “Offer to Purchase”) and the related Letter of Transmittal (the “Letter of Transmittal”). The Offers will expire at 11:59 p.m., New York City time, on December 19, 2016, unless extended or earlier terminated by the Company (the “Expiration Date”). Tenders of Notes may be withdrawn at any time at or prior to 5:00 p.m., New York City time, on December 5, 2016 (the “Withdrawal Deadline”), but may not be withdrawn thereafter except in certain limited circumstances where additional withdrawal rights are required by law.
(3) The Hypothetical Total Consideration is inclusive of the Early Tender Premium (as defined below) but exclusive of accrued and unpaid interest from the last interest payment date applicable to the relevant series of Notes up to, but not including, the Early Settlement Date (as defined below) and is based on the reference yield of the Reference U.S. Treasury Security as of 11:00 a.m., New York City time, on November 18, 2016. The actual reference yields of the Reference U.S. Treasury Securities will be determined by the dealer managers based on certain quotes available at 11:00 a.m., New York City time, on the price determination date, which is expected to be December 6, 2016.

The consideration paid in the applicable Offer for each series of Notes that are validly tendered and accepted for purchase will be determined in the manner described in the Offer to Purchase by reference to a fixed spread over the yield to maturity of the applicable U.S. Treasury Security specified in the table above and in the Offer to Purchase (the “Total Consideration”). Holders of Notes that are validly tendered and not validly withdrawn at or prior to 5:00 p.m., New York City time, on December 5, 2016 (the “Early Tender Deadline”) and accepted for purchase will receive the applicable Total Consideration, which includes an early tender premium of $30.00 per $1,000 principal amount of the Notes accepted for purchase (the “Early Tender Premium”). Holders of Notes who validly tender their Notes following the Early Tender Deadline and on or prior to the Expiration Date will only receive the applicable “Tender Offer Consideration” per $1,000 principal amount of any such Notes validly tendered by such holders that are accepted for purchase, which is equal to the applicable Total Consideration minus the Early Tender Premium. The Total Consideration will be determined at 11:00 a.m., New York City time, on December 6, 2016, unless extended by the Company.

Payments for Notes purchased will include accrued and unpaid interest from the last interest payment date applicable to the relevant series of Notes up to, but not including, the applicable settlement date for such Notes accepted for purchase.

The settlement date for Notes that are validly tendered and not validly withdrawn on or prior to the Early Tender Deadline and accepted for purchase is expected to be December 13, 2016 (the “Early Settlement Date”). The settlement date for Notes that are validly tendered following the Early Tender Deadline but on or prior to the Expiration Date and accepted for purchase is expected to be December 20, 2016, the first business day after the Expiration Date (the “Final Settlement Date”), assuming the Maximum Tender Amount of Notes is not purchased on the Early Settlement Date.

Subject to the applicable tender caps specified in the table above (the “Tender Caps”), the Maximum Tender Amount and proration, all Notes validly tendered and not validly withdrawn on or before the Early Tender Deadline having a higher Acceptance Priority Level (with 1 being the highest) will be accepted before any validly tendered Notes having a lower Acceptance Priority Level (with 5 being the lowest), and all Notes validly tendered after the Early Tender Deadline having a higher Acceptance Priority Level will be accepted before any Notes validly tendered after the Early Tender Deadline having a lower Acceptance Priority Level. However, even if the Offers are not fully subscribed as of the Early Tender Deadline, subject to the Tender Caps, the Maximum Tender Amount and proration, Notes validly tendered and not validly withdrawn on or before the Early Tender Deadline will be accepted for purchase in priority to Notes validly tendered after the Early Tender Deadline even if such Notes validly tendered after the Early Tender Deadline have a higher Acceptance Priority Level than Notes validly tendered prior to the Early Tender Deadline. Subject to applicable law, the Company may increase or decrease any Tender Cap without extending the Early Tender Deadline or the Withdrawal Deadline.

Notes of a series may be subject to proration (rounded to avoid the purchase of Notes in a principal amount other than in an integral multiple of $1,000) if the aggregate principal amount of the Notes of such series validly tendered and not validly withdrawn is greater than the applicable Tender Cap or would cause the Maximum Tender Amount to be exceeded. Furthermore, if the Offers are fully subscribed as of the Early Tender Deadline, holders who validly tender Notes following the Early Tender Deadline will not have any of their Notes accepted for payment regardless of Acceptance Priority Level. The Company’s obligation to accept for payment and to pay for the Notes validly tendered in the Offers is subject to the satisfaction or waiver of the conditions, including a financing condition, as described in the Offer to Purchase. The Company reserves the absolute right, subject to applicable law, to: (i) waive any and all conditions to the Offers, including, without limitation, the financing condition; (ii) extend or terminate the Offers; (iii) increase or decrease the Maximum Tender Amount and/or increase, decrease or eliminate one or more of the Tender Caps without extending the Early Tender Deadline or the Withdrawal Deadline; or (iv) otherwise amend the Offers in any respect.

Information Relating to the Offers

J.P. Morgan Securities LLC and Wells Fargo Securities, LLC are acting as the dealer managers for the Offers. The information agent and tender agent for the Offers is D.F. King & Co, Inc. Copies of the Offer to Purchase, Letter of Transmittal and related offering materials are available by contacting D.F. King & Co, Inc. by telephone at (888) 564‑8149 (toll-free) or (212) 269‑5550 (banks and brokers) or by email at zbh@dfking.com. Questions regarding the Offers should be directed to J.P. Morgan Securities LLC, Liability Management Group, at (212) 834-3424 (collect) or (866) 834-4666 (toll-free) or Wells Fargo Securities, LLC, Liability Management Group, at (704) 410-4760 (collect) or (866) 309-6316 (toll‑free).

This press release shall not constitute an offer to sell, a solicitation to buy or an offer to purchase or sell any securities. The Offers are being made only pursuant to the Offer to Purchase and only in such jurisdictions as is permitted under applicable law.

About Zimmer Biomet

Founded in 1927 and headquartered in Warsaw, Indiana, Zimmer Biomet is a global leader in musculoskeletal healthcare. We design, manufacture and market orthopaedic reconstructive products; sports medicine, biologics, extremities and trauma products; office based technologies; spine, craniomaxillofacial and thoracic products; dental implants; and related surgical products.

We collaborate with healthcare professionals around the globe to advance the pace of innovation. Our products and solutions help treat patients suffering from disorders of, or injuries to, bones, joints or supporting soft tissues. Together with healthcare professionals, we help millions of people live better lives.

We have operations in more than 25 countries around the world and sell products in more than 100 countries. For more information, visit www.zimmerbiomet.com, or follow Zimmer Biomet on Twitter at www.twitter.com/zimmerbiomet.

Cautionary Statement Regarding Forward-Looking Statements

This communication contains forward-looking statements within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995 regarding the cash tender offers for certain outstanding senior notes of the Company. Forward‑looking statements may be identified by the use of forward-looking terms such as “may,” “will,” “expects,” “believes,” “anticipates,” “plans,” “estimates,” “projects,” “assumes,” “guides,” “targets,” “forecasts,” and “seeks” or the negatives of such terms or other variations on such terms or comparable terminology. Such statements are based upon the current beliefs and expectations of management and are subject to significant risks and uncertainties that could cause actual outcomes and results to differ materially. For a list and description of some of such risks and uncertainties, see the Company’s periodic reports filed with the Securities and Exchange Commission (the “SEC”). These factors should not be construed as exhaustive and should be read in conjunction with the other cautionary statements that are included in the Company’s filings with the SEC. The Company disclaims any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as may be set forth in its periodic reports. Accordingly, such forward‑looking statements speak only as of the date made. Readers of this communication are cautioned not to place undue reliance on these forward‑looking statements, since, while management believes the assumptions on which the forward-looking statements are based are reasonable, there can be no assurance that these forward-looking statements will prove to be accurate. This cautionary statement is applicable to all forward-looking statements contained in this communication.

Logo – http://photos.prnewswire.com/prnh/20150624/225371LOGO

SOURCE Zimmer Biomet Holdings, Inc.

Related Links

http://www.zimmerbiomet.com

Why Bundled Payments for Joint Replacement May Be Risky for Patients?

By Michael Wong, JD, Co-authored with Lynn Razzano, RN, MSN, ONCC, November 18,2016

According to the Centers for Medicare & Medicaid Services (CMS), hip and knee replacements are the most common inpatient surgery for Medicare beneficiaries. In 2014, there were more than 400,000 procedures, costing more than $7 billion for the hospitalizations. CMS says that there is little consistency across providers in terms of the quality and cost of care for these procedures.

With an aim to improve the consistency of the quality and cost of care among providers,  CMS has introduced a new payment model, Comprehensive Care for Joint Replacement (CJR), in April 2016, using a concept known as bundled payments.

A significant aspect of this new model is that it contains exceptions to what will be reimbursed—exceptions that could prove potentially harmful to patients recovering from hip and knee replacements. Reconsidering these exceptions could go a long way in improving patient safety, reducing the number of readmissions, and reducing the cost of care for patients undergoing hip and knee replacement.

Comprehensive care for joint replacement (CJR): How it works

To understand how CJR works and its implications on patient care, it is helpful to understand how the system currently operates.

Consider a scenario:

A patient is admitted to a hospital and the doctor recommends undergoing surgery for major joint replacement (the example would also hold true in the event of the reattachment of a lower extremity). The patient goes into surgery, is then hospitalized after the operation, gets discharged, and continues her recovery from home.

The quality and cost of this episode of care—surgery, hospitalization, and recovery—varies considerably from hospital to hospital. For instance, according to the CMS, the rate of complications (e.g., infections, implant failures) can be three times as high at some hospitals, putting those patients cared for at increased risk. Simultaneously, the cost could range anywhere from $16,500 to $33,000 under the current fee-for-service model.

Under the CJR model, CMS provides bundled payments to hospitals for these kinds of surgeries. Bundled payment is the reimbursement of healthcare providers based on the expected costs of a clinically-defined episode of care like the one described above. It has been estimated that one-third of healthcare costs recovered by hospitals are through bundled payments, and that figure is increasing.

With CJR, CMS reimbursement includes all related items and services paid under Medicare Part A (e.g., inpatient hospital care, skilled nursing facility, hospice, lab tests, surgery, and home health care) and under Medicare Part B (e.g. outpatient care, durable medical equipment, home health care, and some preventive services), with certain exceptions.

 

 

READ THE REST HERE

 

SHS invests in innovative 3D printing specialist – Emerging Implant Technologies (EIT) receives growth financing

TÜBINGEN & TUTTLINGEN, Germany–(BUSINESS WIRE)–SHS Gesellschaft für Beteiligungsmanagement mbH is investing in EIT Emerging Implant Technologies GmbH. EIT was established in Tuttlingen, Germany in 2014 and manufactures spinal implant cages using 3D printing technology. SHS is investing funds from its fourth fund generation to finance EIT’s international growth and development of its innovative products.

3D printing, which is also known as additive manufacturing, is used to manufacture cellular and porous implants of biocompatible titanium. These implants mimic the structure and stiffness of natural bone material more accurately than implants manufactured using traditional methods. This in turn promotes bone ingrowth following fusion operations to achieve better clinical results and reduce complication rates. In addition to this, the implants can be fitted on a patient-specific basis, which serves to increase the contact surface and reduce future risks.

“Our EIT Cellular Titanium implants provide the answer to current challenges in implant design and choice of materials as well the extreme cost pressure in medical technology. The additive manufacturing technology allows us to tackle existing problems with new solutions. Thus we can improve the benefits for patients without increasing costs, which is a clear competitive advantage”, explains Guntmar Eisen, founder and CEO of EIT. “This ensures a high level of patient satisfaction and excellent clinical results. We are looking forward to pushing ahead with our international growth, especially in the United States, and our product development with our new partner SHS.”

“EIT’s 3D-printed spine implants have already proven their superior functionality many times in practical applications, thus promoting EIT’s growth”, adds Dr. Bernhard Schirmers, Managing Partner at SHS Gesellschaft für Beteiligungsmanagement. “EIT Emerging Implant Technologies’ management team is experienced and successful in the field of spine surgery. As a medical technology investor, we look forward to supporting them on their path to increased growth.”

“With SHS, EIT is gaining a shareholder with extensive experience in this industry. Together we can enter the next stage of EIT’s growth. This includes development of the company’s innovative product portfolio as well as entering new countries”, says Guy Selbherr, Managing Director of MBG Mittelständische Beteiligungsgesellschaft Baden-Württemberg.

With a total volume of 125 million euro, the fourth SHS fund is focusing on expansion financing, changes in shareholder structures and successor situations. The Tübingen based investor is planning further acquisitions and investments in the fast-growing medical technology and life-science industries in Germany, Austria and Switzerland in the months ahead.

About EIT Emerging Implant Technologies GmbH:

EIT is the first medical device manufacturer in the orthopedic field to exclusively focus on implants that are designed and produced with additive manufacturing methods.

EIT pushes the boundaries of traditional implant manufacturing to obtain versatile, anatomically designed porous implants with increased functionality and maximal bone ingrowth capabilities for all spinal segments.

The EIT implants made of EIT Cellular Titanium® address the shortcomings of the current designs and materials, thereby ensuring optimal clinical outcomes and maximum patient satisfaction.

EIT provides a complete spinal fusion cage portfolio. Patient specific implants to help in the treatment of complex spinal disorders as well as other interesting implant concepts are in development.

EIT consists of a team of skilled and dedicated professionals with a diverse background in management, research and development and quality assurance. The team has a proven track record setting up and managing innovative spinal implant companies, and has developed an extensive network of contacts over many years including internationally renowned surgeons and opinion leaders in the field of spine surgery.

For further information, visit www.eit-spine.de/

About SHS Gesellschaft für Beteiligungsmanagement mbH

SHS Gesellschaft für Beteiligungsmanagement is based in Tübingen, Germany and invests in medical technology and life science companies with a focus on expansion financing, changes in shareholder structures and successor situations. SHS holds minority as well as majority interests. SHS was founded in 1993 and has since gained extensive experience as industry investor, which supports the growth of its portfolio companies through a network of partnerships regarding the introduction of new products, regulatory issues or entering new markets. The SHS fund’s German and international investors include about the European Investment Fund, professional pension insurers, retirement funds, funds of funds, family offices, entrepreneurs and the SHS management team. The AIFM-registered company is currently investing from its fourth generation of funds, for which investors have provided 125 million euro. Equity of up to 20 million euro is invested. Transactions can be carried out in the mid double-digit million range together with a network of co-investors. Reinhilde Spatscheck, Dr. Bernhard Schirmers, Hubertus Leonhardt and Uwe Steinbacher are the Managing Partners at SHS.

Further information: www.shs-capital.eu