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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K912654
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Omnifit PSL M/S 3-Hole Cup, 48MM; Stryker Orthopaedics, Uses in primary and revision total hip ... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
Omnifit PSL M/S 3-Hole Cup, 50MM; Stryker Orthopaedics, Uses in primary and revision total hip ... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
Omnifit PSL M/S 3-Hole Cup, 54MM; Stryker Orthopaedics, Uses in primary and revision total hip ... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
Omnifit M/S PSL Porous Coated Acetabular Shell 54MM; Stryker Orthopaedics, Uses in primary and r... 2 02/07/2011 Stryker Howmedica Osteonics Corp.
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