FDA 510(k), K002172, POLY-TAPES (VARIOUS SIZES AND WOVEN CONSTRUCTION VARIANTS)
FDA 510(k), K002172, POLY-TAPES (VARIOUS SIZES AND WOVEN CONSTRUCTION VARIANTS)
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510(K) Number: K002172
Device Name: POLY-TAPES (VARIOUS SIZES AND WOVEN CONSTRUCTION VARIANTS)
Manufacturer: XIROS PLC
Device Classification Name: suture, nonabsorbable, synthetic, polyethylene
Regulation Number: 878.5000
Classification Product Code: GAT
Date Received: 07/19/2000
Decision Date: 08/28/2001
Regulation Medical Specialty: General & Plastic Surgery
Device Name: POLY-TAPES (VARIOUS SIZES AND WOVEN CONSTRUCTION VARIANTS)
Manufacturer: XIROS PLC
Device Classification Name: suture, nonabsorbable, synthetic, polyethylene
Regulation Number: 878.5000
Classification Product Code: GAT
Date Received: 07/19/2000
Decision Date: 08/28/2001
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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