Medical Device Recalls
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1 result found
510(K) Number: K071638 |
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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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Tapered HD Upgrade Set, REF TSKHDUS, Non-Sterile, Rx Only, Product Usage Usage: Surgical inst... | 2 | 05/12/2015 | BioHorizons Implant Systems Inc |
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