Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K030055 |
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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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Mallory/Head Primary Hip System; Size 11, 160 mm, Lateralized Femoral Stem; Ti-6Al-4V; Porous Plasma... | 3 | 06/11/2015 | Biomet, Inc. |
Mallory Head 4 Finned Acetabular Shell 50 mm, PN 13-104150, hip prosthesis component (Ringloc) | 2 | 02/17/2015 | Biomet, Inc. |
Various Hip systems, Item Nos. 104207 104212 104215 11-162809 11-162810 11-162811 11-162812 1... | 2 | 11/22/2019 | Zimmer Biomet, Inc. |
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