Medical Device Recalls
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1 result found
510(K) Number: K110632 |
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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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Ti-Bond Marketing Literature/Labeling, Catalog No. LT10000, MP-14000 This device is intended to be ... | 2 | 01/05/2015 | Spinal Elements, Inc |
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