Kirschner Medical Corp. - FDA 510(k) Cleared Devices
76
Total
57
Cleared
0
Denied
Kirschner Medical Corp. has 57 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 57 cleared submissions from 1983 to 1995.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
76 devices
Cleared
Aug 29, 1995
KIRSCHNER(R) MODULAR II-C(TM) TOTAL SHOULDER SYSTEM
Orthopedic
568d
Cleared
Jan 18, 1995
KIRSCHNER PERFORMANCE POSTERIOR STABILIZED TOTAL KNEE SYSTEM
Orthopedic
384d
Cleared
Nov 02, 1994
SUMMIT TOTAL HIP SYSTEM
Orthopedic
135d
Cleared
Sep 20, 1994
INTEGRITY TOTAL HIP SYSTEM, NON-POROUS
Orthopedic
176d
Cleared
Aug 05, 1994
LINE EXTENSION FOR KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM, POROUS COATED
Orthopedic
364d
Cleared
Jul 18, 1994
KIRSCHNER C-2 OSTEOCAP TOTAL HIP SYSTEM
Orthopedic
217d
Cleared
Jul 13, 1994
KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM POROUS COATED
Orthopedic
292d
Cleared
Jul 13, 1994
KIRSCHNER INTEGRITY ACETABULAR CUP MODIFICATION
Orthopedic
257d
Cleared
May 18, 1994
KIRSCHNER ZIRCONIA FEMORAL HEAD
Orthopedic
230d
Cleared
May 12, 1993
THREADED PINS
Orthopedic
483d
Cleared
Feb 05, 1993
MEDICAM 900 INSUFFLATOR WITH ACCESSORIES
Obstetrics & Gynecology
294d
Cleared
Oct 20, 1992
LESTER PRESS FIT HIP PROSTHESIS
Orthopedic
316d
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