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FDA 510(k), K072113, INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301
FDA 510(k), K072113, INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301
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510(K) Number: K072113
Device Name: INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301
Manufacturer: INTEGRA LIFESCIENCES CORP.
Device Classification Name: wound dressing with animal-derived material(s)
Regulation Number:
Classification Product Code: KGN
Date Received: 08/01/2007
Decision Date: 10/10/2007
Regulation Medical Specialty:
Device Name: INTEGRA FLOWABLE WOUND MATRIX, MODEL FWD301
Manufacturer: INTEGRA LIFESCIENCES CORP.
Device Classification Name: wound dressing with animal-derived material(s)
Regulation Number:
Classification Product Code: KGN
Date Received: 08/01/2007
Decision Date: 10/10/2007
Regulation Medical Specialty:
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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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