Medical Device Recalls
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1 result found
510(K) Number: K113366 |
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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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Leucadia Autolok" Polyaxial Pedicle Screw System. Intended to help provide correction, immobiliza... | 2 | 05/28/2013 | Alphatec Spine, Inc. |
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