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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 20 of 27 Results
ProductCode: JDI Applicant: HOWMEDICA OSTEONICS CORP. Decision Date To: 02/07/2023
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Export all 27 Records to ExcelExport to Excel | Download Files | More About 510(k)
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abg ii modular hip stem HOWMEDICA OSTEONICS CORP. K092406 11/04/2009
modification to: restoration modular system HOWMEDICA OSTEONICS CORP. K050138 03/21/2005
modification to restoration modular system HOWMEDICA OSTEONICS CORP. K040734 08/25/2004
36mm orthinox v40 femoral head components HOWMEDICA OSTEONICS CORP. K031730 08/29/2003
omnifit hfx hip stem series HOWMEDICA OSTEONICS CORP. K031744 08/08/2003
global modular replacement system (gmrs) HOWMEDICA OSTEONICS CORP. K023087 12/16/2002
trident screw hole plug and trident bone spike HOWMEDICA OSTEONICS CORP. K022799 11/21/2002
36mm v40 femoral head components (lfit and non-lfit) HOWMEDICA OSTEONICS CORP. K022077 07/25/2002
36mm c-taper femoral head components (lfit and non-lfit) HOWMEDICA OSTEONICS CORP. K021310 05/21/2002
super eon plus femoral stems HOWMEDICA OSTEONICS CORP. K020989 04/26/2002
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