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

STELKAST UNICONDYLAR KNEE SYSTEM

K Number: K032824 · Decision Nov 13, 2003
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
113
Applicant Total
40
Review Days
64

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
STELKAST UNICONDYLAR KNEE SYSTEM
K Number
K032824
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3520
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Stelkast Company
Date Received
September 10, 2003
Decision Date
November 13, 2003
Product Code
HSX
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
HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer

Similar 510(k) Clearances

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

View all

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
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 →