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

INTEGRITY TOTAL HIP SYSTEM, NON-POROUS

K Number: K941486 · Decision Sep 20, 1994
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
560
Applicant Total
76
Review Days
176

Basic Information

Device Name
INTEGRITY TOTAL HIP SYSTEM, NON-POROUS
K Number
K941486
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KIRSCHNER MEDICAL CORP.
Date Received
March 28, 1994
Decision Date
September 20, 1994
Product Code
JDI
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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Similar 510(k) Clearances

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

View all

Other Clearances by KIRSCHNER MEDICAL CORP.

K Number Device Name
K940537 KIRSCHNER(R) MODULAR II-C(TM) TOTAL SHOULDER SYSTEM
K936274 KIRSCHNER PERFORMANCE POSTERIOR STABILIZED TOTAL KNEE SYSTEM
K942891 SUMMIT TOTAL HIP SYSTEM
K933843 LINE EXTENSION FOR KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM, POROUS COATED
K935951 KIRSCHNER C-2 OSTEOCAP TOTAL HIP SYSTEM
K934589 KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM POROUS COATED
K935206 KIRSCHNER INTEGRITY ACETABULAR CUP MODIFICATION
K934694 KIRSCHNER ZIRCONIA FEMORAL HEAD
K920188 THREADED PINS
K921837 MEDICAM 900 INSUFFLATOR WITH ACCESSORIES
Search all 76 clearances from KIRSCHNER MEDICAL CORP. →