Cleared Traditional

CUSA? Clarity Ultrasonic Surgical Aspirator System

K251162 · Integra LifeSciences Corporation · General & Plastic Surgery
Oct 2025
Decision
176d
Days
Risk

About This 510(k) Submission

K251162 is an FDA 510(k) clearance for the CUSA? Clarity Ultrasonic Surgical Aspirator System, a Instrument, Ultrasonic Surgical, submitted by Integra LifeSciences Corporation (Princeton, US). The FDA issued a Cleared decision on October 8, 2025, 176 days after receiving the submission on April 15, 2025. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K251162 FDA.gov
FDA Decision Cleared SESE
Date Received April 15, 2025
Decision Date October 08, 2025
Days to Decision 176 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code LFL — Instrument, Ultrasonic Surgical
Device Class

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