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

K2M Fenestrated Tap System

K Number: K152872 · Decision Jan 5, 2016
Classifications
1
FEI Numbers
198
Registration Numbers
198
Same Product Code
353
Applicant Total
16
Review Days
97

Basic Information

Device Name
K2M Fenestrated Tap System
K Number
K152872
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
K2M
Date Received
September 30, 2015
Decision Date
January 5, 2016
Product Code
KNW
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KNW Instrument, Biopsy

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