Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K060336 |
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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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Zimmer/CAS Power Cord, Sesamoid Plasty, NA, Zimmer/CAS, Montreal (Quebec), Canada; REF 20-8000-070-1... | 2 | 12/22/2009 | Zimmer Inc. |
Navitrack® System - OS Knee Universal, Orthopedic Stereotaxic Instrument | 3 | 05/12/2017 | Orthosoft, Inc. dba Zimmer CAS |
Navitrack System - OS Knee Universal, Stereotaxic instrument | 2 | 05/12/2017 | Orthosoft, Inc. dba Zimmer CAS |
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