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

BENCOX Mirabo Cup System

K Number: K220468 · Decision May 18, 2022
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
560
Applicant Total
33
Review Days
90

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Basic Information

Device Name
BENCOX Mirabo Cup System
K Number
K220468
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Corentec Co., Ltd.
Date Received
February 17, 2022
Decision Date
May 18, 2022
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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Other Clearances by Corentec Co., Ltd.

K Number Device Name
K250889 EXULT Knee Replacement System
K242401 EXULT Knee Replacement System
K242046 EXULT Knee Replacement System
K223828 BENCOX Delta Option Heads
K223223 BENCOX Mirabo Z Cup Cortinium
K222278 LOSPA TKR System Instrumentation, EXULT TKR System Instrumentation
K210614 BENCOX Mirabo Z Cup Cortinium
K212034 LOSPA TKR System
K211866 Bencox THR System
K201851 EXULT Femoral component trial - Left, EXULT Femoral component trial - Right
Search all 33 clearances from Corentec Co., Ltd. →