Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K121936 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| NavioPFSTM System, Orthopedic Sterotaxic Instrument, model #'s NPFS-02000, NPFS-02010, NPFS 02020. | 2 | 05/09/2014 |
FEI # 3010266064 Blue Belt Technologies MN |
| NAVIO Soft Tissue Protector, included in instrument kits. The NAVIO Tissue Protector is a reusab... | 2 | 04/01/2020 |
FEI # 1020279 Smith & Nephew, Inc. |
-







