Medical Device Recalls
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1 result found
510(K) Number: K043500 |
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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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Functional Anaesthetic Discography (F.A.D.) Catheter System, Catalog #: D01A, Kyphon, Inc., Sunnyv... | 2 | 02/05/2008 | Kyphon Inc |
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