Medical Device Recalls
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1 result found
510(K) Number: K820777 |
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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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ANSPACH***REF SP-4605-00***Arthroscopic Suture Anchor assembly with Suture Threader***Rx Only*** ... | 2 | 06/25/2014 | The Anspach Effort, Inc. |
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