FDA 510(k), K120506, PARIETEX COMPOSITE VENTRAL PATCH
FDA 510(k), K120506, PARIETEX COMPOSITE VENTRAL PATCH
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510(K) Number: K120506
Device Name: PARIETEX COMPOSITE VENTRAL PATCH
Manufacturer: SOFRADIM PRODUCTION
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 02/21/2012
Decision Date: 06/13/2012
Regulation Medical Specialty: General & Plastic Surgery
Device Name: PARIETEX COMPOSITE VENTRAL PATCH
Manufacturer: SOFRADIM PRODUCTION
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 02/21/2012
Decision Date: 06/13/2012
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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