FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Percuvance Percutaneous Surgical System

K Number: K181852 · Decision Oct 12, 2018
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
64
Review Days
93

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Basic Information

Device Name
Percuvance Percutaneous Surgical System
K Number
K181852
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Teleflexmedical, Inc.
Date Received
July 11, 2018
Decision Date
October 12, 2018
Product Code
GEI
Advisory Committee
General, Plastic Surgery
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

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