Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K073375 |
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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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INTEGRA SURFIX ALPHA Screwdriver Torx 10, REF 219 135 ND | 2 | 02/01/2022 | Smith & Nephew, Inc. |
Integra Newdeal SURFIX Fixed Angle Locking Screw 3.5mm x 22mm (catalog number 285322S) and 3.5mm x 3... | 2 | 06/02/2014 | Integra LifeSciences Corporation |
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