Medical Device Recalls
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1 result found
510(K) Number: K051640 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| U2 Total Knee System Tibial Insert, Posterior Stabilized, #3, 11mm Thick Catalogue number 2303-3032... | 2 | 03/19/2018 |
FEI # 1000395711 United Orthopedic Corporation |
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