Medical Device Recalls
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1 result found
510(K) Number: K141762 |
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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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PerFuse Decompression Instrument PN: 800-0541, Lot:100650. Designed to access the femoral head for ... | 2 | 05/25/2016 | Biomet, Inc. |
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