Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K113561 |
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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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The TM Ardis Interbody System Inserter Stainless Steel, Rubber, Silicone Non Sterile Rx only. The... | 2 | 01/09/2013 | Zimmer, Inc. |
The TM Ardis Interbody System implant is a convex, straight TLIF or PLIF device for interbody fusion... | 3 | 05/10/2017 | Zimmer Trabecular Metal Technology, Inc. |
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