Medical Device Recalls
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1 result found
510(K) Number: K062685 |
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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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ARRAY and POLARIS Spinal System Medium Cross Connector Non Sterile Biomet Spine, Parsippany, NJ. 0... | 2 | 10/22/2010 | Ebi, Llc |
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