Medical Device Recalls
-
1 result found
510(K) Number: K000306 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Pinnacle Cancellous Screw Packaging: Product is housed within a polyurethane protector; this is p... | 2 | 12/19/2012 | DePuy Orthopaedics, Inc. |
-