Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K090234 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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The Spectra-System Dental Implant 2008 system is comprised of dental implant fixtures and prosthetic... | 2 | 03/28/2016 | Implant Direct Sybron Manufacturing, LLC |
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