Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K063569 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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|---|---|---|---|
| Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit | 2 | 12/22/2016 |
FEI # 1038671 Exactech, Inc. |
| Equinoxe Reverse Compression Screw Intended for Primary and Reverse Total Shoulder Arthroplasty. | 2 | 07/31/2012 |
FEI # 1038671 Exactech, Inc. |
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