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U.S. Department of Health and Human Services

510(k) Premarket Notification
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31 to 40 of 49 Results
ProductCode: JDI Applicant: HOWMEDICA OSTEONICS CORP Decision Date To: 05/10/2024
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system 12 x3 acetabular inserts; series ii x3 acetabular inserts HOWMEDICA OSTEONICS CORP K052748 12/02/2005
restoration modular system HOWMEDICA OSTEONICS CORP K051363 06/23/2005
modification to: restoration modular system HOWMEDICA OSTEONICS CORP. K050138 03/21/2005
trident acetabular system HOWMEDICA OSTEONICS CORP K033716 02/10/2005
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
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