Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K083070 |
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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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Ziptight Ankle Syndesmosis Fixation Device, Titanium Implant Titanium Implant for surgical repairs o... | 2 | 03/01/2018 | Zimmer Biomet, Inc. |
Various trauma and sports medicine instruments and implants. Fastener, fixation, nondegradable, sof... | 2 | 05/26/2016 | Biomet, Inc. |
Artificial ligament fixation device # 7PE ZIPLOOP Extended Toggle, Sterile, REF 904755, Biomet Spor... | 2 | 07/01/2010 | Biomet, Inc. |
Toggleloc Artificial ligament fixation device ZIPLOOP Technology Implant Kit, Sterile, REF 909848, ... | 2 | 07/01/2010 | Biomet, Inc. |
Toggleloc System, Biomet Ziptight Ankle Syndesmosis Fixation System - Titanium with Ziploop Technolo... | 2 | 12/22/2009 | Biomet, Inc. |
Toggleloc System, Biomet Ziptight Ankle Syndesmosis Fixation System - SS with Ziploop Technology, po... | 2 | 12/22/2009 | Biomet, Inc. |
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