• FDA 510(k) records for SONICAID SYSTEM 8002 K992607
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FDA 510(k) K150682, CUSA Excel+, by Integra Lifesciences Corp.

FDA 510(k) K150682, CUSA Excel+, by Integra Lifesciences Corp.

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510(K) Number: K150682
Device Name: CUSA Excel+
Manufacturer: Integra Lifesciences Corp.
Device Classification Name: Instrument, Ultrasonic Surgical
Regulation Number: LFL
Classification Product Code: KXA
Date Received: 03/17/2015
Decision Date: 12/18/2015
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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