Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K131591 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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SCFE Driver (SCF-MLD273 & SCF-MLD265) instrument used for the insertion of the Free Gliding SCFE Scr... | 2 | 11/20/2015 | Pega Medical Inc. |
Slipped Capital Femoral Epiphysis (SCFE) Drivers of the Free-Gliding SCFE Screw System with catalogu... | 2 | 06/26/2015 | Pega Medical Inc. |
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