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

PROFORM HIP SYSTEM

K Number: K934161 · Decision Mar 10, 1994
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
22
Applicant Total
40
Review Days
195

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Basic Information

Device Name
PROFORM HIP SYSTEM
K Number
K934161
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stelkast Company
Date Received
August 27, 1993
Decision Date
March 10, 1994
Product Code
JDO
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
JDO Device, Fixation, Proximal Femoral, Implant

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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
K063211 PROVEN KNEE SYSTEM HIGH FLEXION TIBIAL INSERT
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
Search all 40 clearances from Stelkast Company →