Pega Medical Inc.
7 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| SCFE Driver (SCF-MLD273 & SCF-MLD265) instrument used for the insertion of the Free Glidin recall (Z-0324-2016) | Pega Medical Inc. | 2015-11-20 |
| Slipped Capital Femoral Epiphysis (SCFE) Drivers of the Free-Gliding SCFE Screw System wit recall (Z-1848-2015) | Pega Medical Inc. | 2015-06-26 |
| Female Driver, Part number FDr101, instrument used for the insertion of the Fassier-Duval recall (Z-1546-2015) | Pega Medical Inc. | 2015-04-29 |
| GAP Nail 4.8mm (diameter size) of the GAP ENDO-EXO MEDULLARY SYSTEM. Catalog number GAP-N4 recall (Z-1362-2015) | Pega Medical Inc. | 2015-04-02 |
| Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant. Catalogue numbe recall (Z-1472-2014) | Pega Medical Inc. | 2014-04-18 |
| Pega Medical Inc., Fassier-Duval IM Telescopic System, male component (solid shaft), Part recall (Z-1448-2014) | Pega Medical Inc. | 2014-04-10 |
| Male Driver 4.0mm (catalog # MDr140L) and Male Driver 3.2mm (catalog # MDr132L), an instru recall (Z-1494-2011) | Pega Medical Inc. | 2011-03-02 |
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Every clearance here is in the API, with alerts when new ones post.