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

SureClip

K Number: K150936 · Decision Oct 23, 2015
Classifications
1
FEI Numbers
112
Registration Numbers
112
Same Product Code
175
Applicant Total
82
Review Days
199

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Basic Information

Device Name
SureClip
K Number
K150936
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Conmed Corporation
Date Received
April 7, 2015
Decision Date
October 23, 2015
Product Code
FZP
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
FZP Clip, Implantable

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