Medical Device Recalls
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1 result found
510(K) Number: K062216 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW, QTY: (1), STERILE R, REF 71801306 Orthoped... | 2 | 04/18/2017 | Smith & Nephew, Inc. |
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