Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K060694 |
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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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Modular Hybrid Glenoid Base Large for the Comprehensive Shoulder System, The product is placed into ... | 2 | 06/01/2017 | Zimmer Biomet, Inc. |
various polyethylene implants Extremities, Shoulders and Elbows BioModular Shoulder System; Compr... | 2 | 03/27/2017 | Zimmer Biomet, Inc. |
PT113950 PT HYBRID Glenoid Post Regenerex porous titanium construct Sterile R Prosthesis, Shoul... | 2 | 01/09/2013 | Biomet, Inc. |
Biomet Hybrid Glenoid Boss Cutter; item 406150. - Surgical instrument used to prepare the natural sh... | 2 | 09/16/2008 | Biomet, Inc. |
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