Medical Device Recalls
-
1 result found
510(K) Number: K071639 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Large QWIX Compression screw, dia. 7.5 mm L 90 mm, Lot No. FH86, Rx only, Product Usage: The QW... | 2 | 08/19/2016 | Integra LifeSciences Corp. |
-