Kirschner Medical Corp.

FDA Regulatory Profile

Kirschner Medical Corp. appears in FDA public data with 0 recalls, 76 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Aug 29, 1995.

Summary

Total Recalls
0
510(k) Clearances
76
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K940537KIRSCHNER(R) MODULAR II-C(TM) TOTAL SHOULDER SYSTEMAug 29, 1995
K936274KIRSCHNER PERFORMANCE POSTERIOR STABILIZED TOTAL KNEE SYSTEMJan 18, 1995
K942891SUMMIT TOTAL HIP SYSTEMNov 2, 1994
K941486INTEGRITY TOTAL HIP SYSTEM, NON-POROUSSep 20, 1994
K933843LINE EXTENSION FOR KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM, POROUS COATEDAug 5, 1994
K935951KIRSCHNER C-2 OSTEOCAP TOTAL HIP SYSTEMJul 18, 1994
K935206KIRSCHNER INTEGRITY ACETABULAR CUP MODIFICATIONJul 13, 1994
K934589KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM POROUS COATEDJul 13, 1994
K934694KIRSCHNER ZIRCONIA FEMORAL HEADMay 18, 1994
K920188THREADED PINSMay 12, 1993
K921837MEDICAM 900 INSUFFLATOR WITH ACCESSORIESFeb 5, 1993
K915500LESTER PRESS FIT HIP PROSTHESISOct 20, 1992
K912837MCAFEE SPINAL SYSTEM FOR POSTERIOR APPLICATIONSAug 26, 1992
K922544MEDICAM 900 AUTOELECTRONIC LIGHT SOURCEAug 7, 1992
K921672INTER-HA HIP PROSTHESISAug 7, 1992
K914675MODULAR FEMORAL HEAD WITH OFFSET TRUNIONAug 7, 1992
K920396KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEMAug 7, 1992
K901507MCAFFEE UNIVERSAL SPINAL SYSTEM (MUSS)Jan 28, 1992
K913492KIRSCHNER(R) HYBRIDFIT TOTAL KNEE SYSTEMDec 27, 1991
K913632BATEMAN UPF-III BIPOLAR ENDOPROSTHESIS SYSTEMNov 13, 1991