FDA 510(k), K183184, FlareHawk Interbody Fusion System

FDA 510(k), K183184, FlareHawk Interbody Fusion System

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510(K) Number: K183184
Device Name: FlareHawk Interbody Fusion System
Manufacturer: Integrity Implants Inc
Device Classification Name: intervertebral fusion device with bone graft, lumbar
Regulation Number: 888.3080
Classification Product Code: MAX
Date Received: 11/19/2018
Decision Date: 04/03/2019
Regulation Medical Specialty: Orthopedic

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