Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K172194 |
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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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ORTHOFIX, Connector System, LARGE SET SCREW, REF 79-2002 | 2 | 04/11/2018 | Orthofix, Inc |
ORTHOFIX, Connector System, SMALL SET SCREW, REF 79-2003 | 2 | 04/11/2018 | Orthofix, Inc |
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