Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K123485 |
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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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Various trauma and sports medicine instruments and implants. Fastener, fixation, nondegradable, sof... | 2 | 05/26/2016 | Biomet, Inc. |
Juggerknotless Drill Bit, REF 110003173, Sterile, Single Use Product Usage: The Juggerknotless... | 2 | 11/19/2013 | Biomet, Inc. |
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