Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K142814 |
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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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Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151810 | 2 | 08/09/2019 | Zimmer Biomet, Inc. |
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151811 | 2 | 08/09/2019 | Zimmer Biomet, Inc. |
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151815 | 2 | 08/09/2019 | Zimmer Biomet, Inc. |
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151813 | 2 | 08/09/2019 | Zimmer Biomet, Inc. |
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151814 | 2 | 08/09/2019 | Zimmer Biomet, Inc. |
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812 | 2 | 08/09/2019 | Zimmer Biomet, Inc. |
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