Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K122326 |
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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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Tibial Alignment Guide; Orthopedic Stereotaxic Instrument; | 2 | 06/02/2015 | Zimmer CAS |
SmartTools Knee System Orthopedic Stereotaxic Instrument | 2 | 04/19/2017 | Orthosoft, Inc. dba Zimmer CAS |
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