IsoTis OrthoBiologics

/C O R R E C T I O N -- Isotis Inc/

    Irvine, California (ots/PRNewswire) - In the news release, "IsoTis Appoints James P. Abraham as Senior Vice  President Sales" issued on 16 Apr 2007 12:00 GMT, by Isotis Inc nasdaq:ISOT  over PR Newswire, we are advised by a representative of the company that  the release is the same for several wire tasks, so the destinations will be added to this task transmitted by PR Newswire. Complete, corrected release follows:

    IsoTis, Inc. (NASDAQ: ISOT), the orthobiologics company, today announced it has appointed James (Jim) P. Abraham as Senior Vice President of Sales.

    Mr. Abraham successfully served the company in the same capacity from November 2004 until early 2006. He has a 24 year track record in the orthopaedic industry, and as an executive played a key role in growing sales at Sulzer Orthopedics from 1991 to 1994, Encore Medical Corp. from 1994 to 1998, Regeneration Technologies, Inc. from 1998 to 2002, and at IsoTis from 2004 to 2006. Jim Abraham left IsoTis to set up his own consultancy firm that primarily focused on advising a private equity group on M&A and investments in the orthobiology industry. Mr. Abraham replaces Alan Donze who left IsoTis on April 5.

    Pieter Wolters, President and CEO of IsoTis said: "We are very pleased at having succeeded in attracting Jim Abraham to once again take up the responsibility as our Senior Vice President of Sales. Based on our close collaboration in the past and his successful work with our sales team, I am confident that he will provide the leadership to continue to execute our strategy successfully and to help us attain our goals. "

    About IsoTis, Inc.

    IsoTis is a leading orthobiologics company that develops, manufactures and markets proprietary products for the treatment of musculoskeletal diseases and disorders. IsoTis' current orthobiologics products are bone graft substitutes that promote the regeneration of bone and are used to repair natural, trauma-related and surgically-created defects common in orthopedic procedures, including spinal fusions. IsoTis' current commercial business is highlighted by its Accell line of products, which the company believes represents the next generation in bone graft substitution.

    Certain statements in this press release are "forward-looking statements" within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, including those that refer to management's plans and expectations for future operations, prospects and financial condition. Words such as "strategy," "expects," "plans," "anticipates," "believes," "will," "continues," "estimates," "intends," "projects," "goals," "targets" and other words of similar meaning are intended to identify such forward-looking statements. One can also identify them by the fact that they do not relate strictly to historical or current facts. Such statements are based on the current expectations of the management of IsoTis only. Undue reliance should not be placed on these statements because, by their nature, they are subject to known and unknown risks and can be affected by factors that are beyond the control of IsoTis. Actual results could differ materially from current expectations due to a number of factors and uncertainties affecting IsoTis' business, including, but not limited to, a competitive sales and marketing environment, the timely commencement and success of IsoTis' clinical trials and research endeavors, delays in receiving U.S. Food and Drug Administration or other regulatory approvals (a.o. EMEA, CE), including the risk that the FDA determines that our Accell Putty and Accell TBM products are not human tissue or class II medical devices, that the Company is unable to obtain 510(k) clearance for its Accell products, that the FDA requires the Company to obtain premarket approval of its Accell products prior to continuing their marketing, that the FDA requires the Company to produce additional clinical data to support approval or clearance of its products, that the FDA imposes compliance measures against the Company for the marketing of its Accell products, including imposing fines and injunctions or causing the Company to recall its Accell products, market acceptance of IsoTis' products, effectiveness of IsoTis' distribution channels, development of competing therapies and/or technologies, the terms of any future strategic alliances, the need for additional capital, the inability to obtain, or meet, conditions imposed for required governmental and regulatory approvals and consents. IsoTis expressly disclaims any intent or obligation to update these forward-looking statements except as required by law. For a more detailed description of the risk factors and uncertainties affecting IsoTis, refer to the Annual Report on Form 20-F for the fiscal year ended December 31, 2005 of IsoTis SA, the predecessor of the Company, filed with the SEC, to IsoTis SA's reports filed from time to time with the Swiss Stock Exchange (SWX), Euronext Amsterdam N.V., SEDAR at www.sedar.com and the Toronto Stock Exchange (TSX), and to the reports filed from time to time by the Company with the SEC.

ots Originaltext: Isotis Inc
Im Internet recherchierbar: http://www.presseportal.ch

Contact:
For information contact: Rob Morocco, CFO, +1-(949)-855-7155,
robert.morocco@isotis.com. Hans Herklots, Director IR,
+1-(949)-855-7195 or +41-(21)-620-6011, hans.herklots@isotis.com



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