Medical Device Recalls
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1 result found
510(K) Number: K112069 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device. | 2 | 12/12/2023 | Encore Medical, LP |
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