Medical Device Recalls
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1 result found
510(K) Number: K133746 |
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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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| Polaris 4.75 TI Spinal System, 4.0 x 20 MM, Closed MAS, Closed Head Multiaxial Screw, Non-Sterile, R... | 2 | 07/20/2015 | Biomet Spine, LLC |
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