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FDA 510(k), K161737, RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed
FDA 510(k), K161737, RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed
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510(K) Number: K161737
Device Name: RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed
Manufacturer: MYCO MEDICAL
Device Classification Name: suture, surgical, absorbable, polydioxanone
Regulation Number: 878.4840
Classification Product Code: NEW
Date Received: 06/23/2016
Decision Date: 03/02/2017
Regulation Medical Specialty: General & Plastic Surgery
Device Name: RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed
Manufacturer: MYCO MEDICAL
Device Classification Name: suture, surgical, absorbable, polydioxanone
Regulation Number: 878.4840
Classification Product Code: NEW
Date Received: 06/23/2016
Decision Date: 03/02/2017
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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