Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K193373 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Comprehensive Reverse Shoulder System, Item numbers 115394, 115395, 115396, 115398, 180550, 180551, ... | 2 | 12/17/2020 | Biomet, Inc. |
Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper Adapter-Shoulder Prosthe... | 2 | 10/09/2020 | Biomet, Inc. |
-