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FDA 510(k), K060713, PROCEED SURGICAL MESH
FDA 510(k), K060713, PROCEED SURGICAL MESH
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510(K) Number: K060713
Device Name: PROCEED SURGICAL MESH
Manufacturer: ETHICON INC.
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 03/17/2006
Decision Date: 05/25/2006
Regulation Medical Specialty: General & Plastic Surgery
Device Name: PROCEED SURGICAL MESH
Manufacturer: ETHICON INC.
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 03/17/2006
Decision Date: 05/25/2006
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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