Medical Device Recalls
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1 result found
510(K) Number: K101085 |
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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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Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemen... | 2 | 03/10/2013 | Spine Smith Partners LP |
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