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FDA 510(k), K112786, PROSERIES BIOIMPLANTS-PROANKLE/PROCUFF
FDA 510(k), K112786, PROSERIES BIOIMPLANTS-PROANKLE/PROCUFF
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510(K) Number: K112786
Device Name: PROSERIES BIOIMPLANTS-PROANKLE/PROCUFF
Manufacturer: SYNOVIS ORTHOPEDIC AND WOUNDCARE, INC.
Device Classification Name: mesh, surgical
Regulation Number: 878.3300
Classification Product Code: FTM
Date Received: 09/26/2011
Decision Date: 10/25/2011
Regulation Medical Specialty: General & Plastic Surgery
Device Name: PROSERIES BIOIMPLANTS-PROANKLE/PROCUFF
Manufacturer: SYNOVIS ORTHOPEDIC AND WOUNDCARE, INC.
Device Classification Name: mesh, surgical
Regulation Number: 878.3300
Classification Product Code: FTM
Date Received: 09/26/2011
Decision Date: 10/25/2011
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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