Medical Device Recalls
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1 result found
510(K) Number: K141478 |
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Product Description
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Recall
Class |
FDA Recall
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Recalling Firm
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Sterile Low Profile Screw, Titanium, 6.7 x 65mm Part Number: AR-8967-2865S - Product Usage: is inte... | 2 | 07/29/2020 | Arthrex, Inc. |
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