Medical Device Recalls
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1 result found
510(K) Number: K093629 |
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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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Solitaire-35 Peek Solitaire Anterior Spinal System. The Solitaire-35 is an intervertebral body fusio... | 2 | 09/27/2013 | Ebi, Llc |
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