Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K110789 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Synthes Application Instrument Sternal Zip Flex System intended for use in primary or secondary c... | 2 | 10/30/2013 | Synthes USA HQ, Inc. |
Synthes Application Instrument for Sternal ZIPFIX. Indications for use include primary or secondar... | 2 | 11/14/2015 | Synthes (USA) Products LLC |
Synthes Application Instrument for Sternal ZIPFIX; indications for use include primary or secondary ... | 2 | 08/27/2015 | Synthes (USA) Products LLC |
-