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FDA 510(k), K133223, XENMATRIX AB SURGICAL GRAFT
FDA 510(k), K133223, XENMATRIX AB SURGICAL GRAFT
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510(K) Number: K133223
Device Name: XENMATRIX AB SURGICAL GRAFT
Manufacturer: C.R. BARD, INC.
Device Classification Name: collagen surgical mesh containing drugs
Regulation Number: 878.3300
Classification Product Code: PIJ
Date Received: 10/21/2013
Decision Date: 09/19/2014
Regulation Medical Specialty: General & Plastic Surgery
Device Name: XENMATRIX AB SURGICAL GRAFT
Manufacturer: C.R. BARD, INC.
Device Classification Name: collagen surgical mesh containing drugs
Regulation Number: 878.3300
Classification Product Code: PIJ
Date Received: 10/21/2013
Decision Date: 09/19/2014
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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