Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K912654 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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