Medical Device Recalls
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1 result found
510(K) Number: K170539 |
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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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| Avitus® Bone Harvester w/ Filter Insert - 5mm intended to harvest cancellous bone and bone marrow ... | 2 | 03/23/2019 |
FEI # 3011504993 Avitus Orthopaedics, Inc. |
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