Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K041393 |
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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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Pega Medical Inc., Fassier-Duval IM Telescopic System, male component (solid shaft), Part number: M... | 2 | 04/10/2014 | Pega Medical Inc. |
Male Driver 4.0mm (catalog # MDr140L) and Male Driver 3.2mm (catalog # MDr132L), an instrument used ... | 2 | 03/02/2011 | Pega Medical Inc. |
Female Driver, Part number FDr101, instrument used for the insertion of the Fassier-Duval IM Telesco... | 2 | 04/29/2015 | Pega Medical Inc. |
Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant. Catalogue number FD-040... | 2 | 04/18/2014 | Pega Medical Inc. |
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