FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

CUSA Clarity Ultrasonic Surgical Aspirator System

K Number: K200774 · Decision Jun 23, 2020
Classifications
1
FEI Numbers
138
Registration Numbers
138
Same Product Code
155
Applicant Total
13
Review Days
90

Basic Information

Device Name
CUSA Clarity Ultrasonic Surgical Aspirator System
K Number
K200774
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Integra LifeSciences Corporation
Date Received
March 25, 2020
Decision Date
June 23, 2020
Product Code
LFL
Advisory Committee
Unknown
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LFL Instrument, Ultrasonic Surgical

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Other Clearances by Integra LifeSciences Corporation

K Number Device Name
K250752 AURORA® Surgiscope® System (ASX15/60); AURORA® Surgiscope® System (ASX15/80)
K240493 CUSA® Clarity Ultrasonic Surgical Aspirator System
K221763 CUSA Clarity Ultrasonic Surgical Aspirator System
K210128 INTEGRA Wound Matrix (Macro-Channels)
K193346 Codman Surgical Patties & Strips
K190588 Integra TITAN Reverse Shoulder System
K190180 CUSA Clarity Ultrasonic Surgical Aspirator System
K182809 CUSA Clarity Ultrasonic Surgical Aspirator System
K182801 Codman Electrosurgical Irrigator, Codman Electrosurgical Irrigator Interconnecting Cable
K173717 Integra TITAN Reverse Shoulder System
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