FDA 510(k), K031332, BARD PELVISOFT ACELLULAR COLLAGEN BIOMESH
FDA 510(k), K031332, BARD PELVISOFT ACELLULAR COLLAGEN BIOMESH
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510(K) Number: K031332
Device Name: BARD PELVISOFT ACELLULAR COLLAGEN BIOMESH
Manufacturer: C.R. BARD, INC.
Device Classification Name: mesh, surgical
Regulation Number: 878.3300
Classification Product Code: FTM
Date Received: 04/28/2003
Decision Date: 05/15/2003
Regulation Medical Specialty: General & Plastic Surgery
Device Name: BARD PELVISOFT ACELLULAR COLLAGEN BIOMESH
Manufacturer: C.R. BARD, INC.
Device Classification Name: mesh, surgical
Regulation Number: 878.3300
Classification Product Code: FTM
Date Received: 04/28/2003
Decision Date: 05/15/2003
Regulation Medical Specialty: General & Plastic Surgery
- 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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