FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

Modified Bencox Hip System

K Number: K150007 · Decision May 4, 2015
Classifications
1
FEI Numbers
271
Registration Numbers
271
Same Product Code
551
Applicant Total
6
Review Days
122

Basic Information

Device Name
Modified Bencox Hip System
K Number
K150007
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Corentec Co., Ltd
Date Received
January 2, 2015
Decision Date
May 4, 2015
Product Code
LPH
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

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