Medical Device Recalls
-
1 to 5 of 5 Results
510(K) Number: K090763 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
stryker MAKO RESTORIS MCK BASEPLATE TRIAL (SIZE 6 RM/LL), REF 170616, intended for use in a Partial ... | 2 | 04/12/2023 | Howmedica Osteonics Corp. |
stryker MAKO RESTORIS MCK BASEPLATE TRIAL (SIZE 5 RM/LL), REF 170615, intended for use in a Partial ... | 2 | 04/12/2023 | Howmedica Osteonics Corp. |
Restoris Multicompartmental Knee (MCK) System is an implant system designed to be used with MAKO's R... | 2 | 03/04/2014 | Mako Surgical Corporation |
Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for single or multi-compa... | 2 | 03/01/2016 | Mako Surgical Corporation |
Restoris MCK Onlay Insert Extractor. | 2 | 06/01/2018 | Mako Surgical Corporation |
-