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FDA 510(k), K131143, TRELLIS COLLAGEN RIBBON
FDA 510(k), K131143, TRELLIS COLLAGEN RIBBON
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$149.00 USD
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510(K) Number: K131143
Device Name: TRELLIS COLLAGEN RIBBON
Manufacturer: WRIGHT MEDICAL TECHNOLOGY, INC.
Device Classification Name: mesh, surgical, collagen, orthopaedics, reinforcement of tendon
Regulation Number: 878.3300
Classification Product Code: OWY
Date Received: 04/23/2013
Decision Date: 10/07/2013
Regulation Medical Specialty: General & Plastic Surgery
Device Name: TRELLIS COLLAGEN RIBBON
Manufacturer: WRIGHT MEDICAL TECHNOLOGY, INC.
Device Classification Name: mesh, surgical, collagen, orthopaedics, reinforcement of tendon
Regulation Number: 878.3300
Classification Product Code: OWY
Date Received: 04/23/2013
Decision Date: 10/07/2013
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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