Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K081867 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
The RIO (TGS 2.), Model # MAKO TGS 2.0 (Part No. 204000). The RIO is intended to assist the surge... | 2 | 11/19/2012 | Mako Surgical Corporation |
200996-Cable Assembly, Hybrid Extended Length, 200997 Cable Assembly, Hybrid, Guidance Module, 20... | 2 | 10/19/2009 | Mako Surgical Corporation |
-