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

CUSA Excel+

K Number: K150682 · Decision Dec 18, 2015
Classifications
1
FEI Numbers
115
Registration Numbers
116
Same Product Code
156
Applicant Total
29
Review Days
276

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Basic Information

Device Name
CUSA Excel+
K Number
K150682
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Integra Lifesciences Corp.
Date Received
March 17, 2015
Decision Date
December 18, 2015
Product Code
LFL
Advisory Committee
Unknown
Review Advisory Committee
SU
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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K131184 INTEGRA LICOX PTO2 MONITOR
K092227 JARIT, RUGGLES, R&B REDMOND/ REDMOND, MILTEX, MEISTERHAND - KERRISON RONGEURS
K092395 OSV II LUMBAR VALVE SYSTEM AND OSV II LOW FLOW LUMBAR VALVE SYSTEM
K081635 INTEGRA MESHED BILAYER WOUND MATRIX
K081401 MAYFIELD MR/X-RAY SKULL CLAMP
Search all 29 clearances from Integra Lifesciences Corp. →