Medical Device Recalls
-
1 to 4 of 4 Results
510(K) Number: K093552 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
EVOLUTION® MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are f... | 2 | 07/01/2024 | MicroPort Orthopedics Inc. |
EVOLUTION MP Tibial Bases, Size 2+ LEFT, REF ETPKN2PL, knee tibial base | 2 | 11/22/2022 | MicroPort Orthopedics Inc. |
EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial base | 2 | 11/22/2022 | MicroPort Orthopedics Inc. |
EVOLUTION MP TIBIAL BASE, REF ETPKN8SR, SIZE 8 RIGHT, TYPE PRIMARY, FIT CEMENTED, STYLE KEELED, STER... | 2 | 03/06/2015 | Microport Orthopedics INC. |
-