Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K052248 |
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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 Brand Name: Distal Radius Fracture Repair System Device Classification Name: Plate, Fixation... | 2 | 08/13/2014 | Biomet, Inc. |
DePuy DNP Anatomic Fracture Repair System, JIG DNP Anatomic, Depuy, Warsaw, IN; REF DNPAJIG. The ... | 2 | 02/11/2009 | Depuy Orthopaedics, Inc. |
DePuy DNP Anatomic Fracture Repair System, DNP Anatomic Right, Depuy, Warsaw, IN; REF DNPAR. The ... | 2 | 02/11/2009 | Depuy Orthopaedics, Inc. |
DePuy DNP Anatomic Fracture Repair System, Locking Screw DNP Anatomic, Depuy, Warsaw, IN; REF DNPALS... | 2 | 02/11/2009 | Depuy Orthopaedics, Inc. |
DePuy DNP Anatomic Fracture Repair System, DNP Anatomic Left, Depuy, Warsaw, IN; REF DNPAL. The d... | 2 | 02/11/2009 | Depuy Orthopaedics, Inc. |
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