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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 14 Results
510(K) Number: K912654
 
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Omnifit M/S PSL Porous Coated Acetabular Shell 40MM; Stryker Orthopaedics, Uses in primary and r... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
Omnifit M/S PSL Porous Coated Acetabular Shell 42MM; Stryker Orthopaedics, Uses in primary and r... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
Omnifit M/S PSL Porous Coated Acetabular Shell 44MM; Stryker Orthopaedics, Uses in primary and r... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
Omnifit M/S PSL Porous Coated Acetabular Shell 46MM; Stryker Orthopaedics, Uses in primary and r... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
Omnifit M/S PSL Porous Coated Acetabular Shell 48MM; Stryker Orthopaedics, Uses in primary and r... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
Omnifit M/S PSL Porous Coated Acetabular Shell 50MM; Stryker Orthopaedics, Uses in primary and r... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
Omnifit PSL M/S 3-Hole Cup, 58MM; Stryker Orthopaedics, Uses in primary and revision total hip ... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
Omnifit M/S PSL Shell 58 MM; Stryker Orthopaedics, Uses in primary and revision total hip arthr... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
Omnifit M/S Dual Geom Shell 58 MM; Stryker Orthopaedics, Uses in primary and revision total hi... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
Omnifit PSL M/S 3-Hole Cup, 46MM; Stryker Orthopaedics, Uses in primary and revision total hip ... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
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