Medical Device Recalls
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1 result found
510(K) Number: K902824 |
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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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Device Name: Terino Square Chin-Style II-Medium; Catalog Number: TSCII-M. To augment or reconstru... | 2 | 09/17/2013 | Implantech Associates Inc |
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