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FDA 510(k), K160136, Flowable Wound Matrix
FDA 510(k), K160136, Flowable Wound Matrix
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510(K) Number: K160136
Device Name: Flowable Wound Matrix
Manufacturer: COOK BIOTECH INCORPORATED
Device Classification Name: Wound Dressing With Animal-Derived Material(S)
Regulation Number:
Classification Product Code: KGN
Date Received: 01/20/2016
Decision Date: 09/28/2016
Regulation Medical Specialty:
Device Name: Flowable Wound Matrix
Manufacturer: COOK BIOTECH INCORPORATED
Device Classification Name: Wound Dressing With Animal-Derived Material(S)
Regulation Number:
Classification Product Code: KGN
Date Received: 01/20/2016
Decision Date: 09/28/2016
Regulation Medical Specialty:
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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