Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K071714 |
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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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Orthosoft Navitrack, OS Unicondylar Knee 1.0 - Universal; software application for orthopedic surgic... | 2 | 03/02/2009 | Zimmer Inc. |
Zimmer/CAS Power Cord, Sesamoid Plasty, NA, Zimmer/CAS, Montreal (Quebec), Canada; REF 20-8000-070-1... | 2 | 12/22/2009 | Zimmer Inc. |
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