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

PROVEN KNEE SYSTEM HIGH FLEXION TIBIAL INSERT

K Number: K063211 · Decision Jan 18, 2007
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
40
Review Days
87

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Basic Information

Device Name
PROVEN KNEE SYSTEM HIGH FLEXION TIBIAL INSERT
K Number
K063211
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stelkast Company
Date Received
October 23, 2006
Decision Date
January 18, 2007
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 Stelkast Company

K Number Device Name
K122883 EXP TIBIAL INSERTS AND PATELLAR COMPONENTS FOR THE PROVEN GEN-FLEX TOTAL KNEE SYSTEM
K122773 CROSS-OVER ACETABULAR SHELL & LINER
K094035 EXP ACETABULAR LINER, MODELS SC3342 NON-HOODED 28MM, SC3343 HOODED 28MM
K081458 PROVEN STEM EXTENDER
K051976 PROVEN REVISION MODULAR TIBIAL TRAY
K033944 STELKAST 32MM MODULAR CERAMIC FEMORAL HEAD
K032824 STELKAST UNICONDYLAR KNEE SYSTEM
K031901 PROVEN REVISION FEMORAL AND PROVEN REVISION TIBIAL INSERT
K032110 PROCLASS PRESS FIT HIP STEM
K030577 PROVEN MODULAR TIBIAL TRAY
Search all 40 clearances from Stelkast Company →