Blue Belt Technologies MN
4 FDA 510(k) clearances · Recalling firm
◉ Watch Blue Belt Technologies MN
| Record | Firm | Date |
|---|---|---|
| Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial. Unicondylar Knee recall (Z-1942-2014) | Blue Belt Technologies MN | 2014-06-27 |
| Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee recall (Z-1943-2014) | Blue Belt Technologies MN | 2014-06-27 |
| NavioPFSTM System, Orthopedic Sterotaxic Instrument, model #'s NPFS-02000, NPFS-02010, NPF recall (Z-1575-2014) | Blue Belt Technologies MN | 2014-05-09 |
| Blue Belt Technologies, Inc. Monitor Drape REF: PFSD-V0001, Rx only, Sterile EO. Product U recall (Z-1995-2013) | Blue Belt Technologies MN | 2013-08-21 |
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Every clearance here is in the API, with alerts when new ones post.