Medical Device Recalls
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1 result found
510(K) Number: K100417 |
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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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Integra XKnife® Stereotactic Radiosurgery and Radiotherapy Treatment Planning, Software Versions 5.... | 2 | 04/12/2013 | Integra LifeSciences Corp. |
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