Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K110592 |
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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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Dynamic Locking Screw System (DLS) 3.7mm & Dynamic Locking Screw (DLS) 5.0mm; intended for use in lo... | 2 | 09/18/2015 | Synthes (USA) Products LLC |
3.7mm and 5.0mm Dynamic Locking Screw (DLS) Product Usage: 3.7mm and 5.0mm Dynamic Locking Scr... | 2 | 11/26/2013 | Synthes USA HQ, Inc. |
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