Medical Device Recalls
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1 result found
510(K) Number: K141253 |
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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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| Modera Modular Pedicle Screw System Shank Insertion Instrument, 3-107-07 | 2 | 08/03/2018 | New Era Orthopaedics, LLc |
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