Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K131792 |
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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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SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Devi... | 2 | 10/11/2018 | Synthes (USA) Products LLC |
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Devi... | 2 | 10/11/2018 | Synthes (USA) Products LLC |
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Devi... | 2 | 10/11/2018 | Synthes (USA) Products LLC |
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Devi... | 2 | 10/11/2018 | Synthes (USA) Products LLC |
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Devi... | 2 | 10/11/2018 | Synthes (USA) Products LLC |
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