Medical Device Recalls
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1 result found
510(K) Number: K121777 |
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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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U2 Acetabular cup, Ti beads porous coated, ®44mm U2 Acetabular cup, Ti beads porous coated, ®46mm ... | 2 | 05/24/2013 | Orthopedic Alliance LLC |
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