Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K093844 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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TWINFIX" Ultra PLLA/HA 6.5 mm with 2 ULTRABRAID" Suture, White / Black: Part Number: 72202608 Bio... | 2 | 09/17/2013 | Smith & Nephew, Inc. Endoscopy Division |
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