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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 19 of 19 Results
ProductCode: KWL Applicant: HOWMEDICA OSTEONICS CORP Decision Date To: 05/17/2024
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Export all 19 Records to ExcelExport to Excel | Download Files | More About 510(k)
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510(K)
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rejuvenate modular hip system HOWMEDICA OSTEONICS CORP K081044 06/03/2008
stryker modular hip system HOWMEDICA OSTEONICS CORP K071082 09/13/2007
corin adaptor sleeve HOWMEDICA OSTEONICS CORP K071471 09/10/2007
restoration modular system HOWMEDICA OSTEONICS CORP K051363 06/23/2005
modification to: restoration modular system HOWMEDICA OSTEONICS CORP. K050138 03/21/2005
modification to restoration modular system HOWMEDICA OSTEONICS CORP. K040734 08/25/2004
omnifit hfx hip stem series HOWMEDICA OSTEONICS CORP. K031744 08/08/2003
unitrax modular unipolar system HOWMEDICA OSTEONICS CORP. K014226 01/25/2002
unitrax c-taper neck adjustment sleeve HOWMEDICA OSTEONICS CORP. K992570 09/01/1999
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