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

KIRSCHNER PERFORMANCE POSTERIOR STABILIZED TOTAL KNEE SYSTEM

K Number: K936274 · Decision Jan 18, 1995
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
76
Review Days
384

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Basic Information

Device Name
KIRSCHNER PERFORMANCE POSTERIOR STABILIZED TOTAL KNEE SYSTEM
K Number
K936274
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kirschner Medical Corp.
Date Received
December 30, 1993
Decision Date
January 18, 1995
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

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Other Clearances by Kirschner Medical Corp.

K Number Device Name
K940537 KIRSCHNER(R) MODULAR II-C(TM) TOTAL SHOULDER SYSTEM
K942891 SUMMIT TOTAL HIP SYSTEM
K941486 INTEGRITY TOTAL HIP SYSTEM, NON-POROUS
K933843 LINE EXTENSION FOR KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM, POROUS COATED
K935951 KIRSCHNER C-2 OSTEOCAP TOTAL HIP SYSTEM
K935206 KIRSCHNER INTEGRITY ACETABULAR CUP MODIFICATION
K934589 KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM POROUS COATED
K934694 KIRSCHNER ZIRCONIA FEMORAL HEAD
K920188 THREADED PINS
K921837 MEDICAM 900 INSUFFLATOR WITH ACCESSORIES
Search all 76 clearances from Kirschner Medical Corp. →