Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K110054 |
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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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NavitrackER Kit A: Knee, Model Number 20-8000-000-07, | 2 | 03/03/2022 | Orthosoft, Inc. dba Zimmer CAS |
Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application in... | 2 | 04/26/2017 | Orthosoft, Inc. dba Zimmer CAS |
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