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

EXULT Knee Replacement System

K Number: K242046 · Decision Aug 1, 2024
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
33
Review Days
20

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Basic Information

Device Name
EXULT Knee Replacement System
K Number
K242046
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Corentec Co., Ltd.
Date Received
July 12, 2024
Decision Date
August 1, 2024
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JWH), ordered by most recent decision date.

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Other Clearances by Corentec Co., Ltd.

K Number Device Name
K250889 EXULT Knee Replacement System
K242401 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
K220468 BENCOX Mirabo Cup System
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. →