Medical Device Recalls
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1 result found
510(K) Number: K110598 |
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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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SMR glenosphere impactor/extractor; Used to implant the glenosphere in the SMR Reverse Shoulder repl... | 2 | 05/25/2016 | Limacorporate S.p.A |
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