Buckman Co., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
111
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K961320CROSS MEDICAL BONE PLATE SYSTEM/ CM BONE PLATE SYSTEM/CROSS TI BONE PLATE SYSTEMJune 25, 1998
K974641FUTURELASE 3000/3002 ERBIUM LASER SYSTEMJune 8, 1998
K964252ORTHOCHUCKMay 27, 1997
K950099SYNERGY(TM) TI POSTERIOR SPINAL SYSTEMJanuary 16, 1997
K960451WEBB-MORLEY SPINE SYSTEMApril 18, 1996
K950999KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESISJanuary 25, 1996
K945756IMAGN(TM) 2000 SYSTEMDecember 19, 1995
K940003VOLUMET CD4 + AND CD8 + T LYMPHOCYTE COUNT TEST KITOctober 19, 1995
K951117LIHTAN 532 LASEROctober 18, 1995
K942751VANGUARD SERIES GAS REGULATORSFebruary 9, 1995
K934429ANTERIOR SPINE SYSTEMOctober 20, 1994
K931778LAPAROSCOPY INSTRUMENTSApril 12, 1994
K921686ENDOMED LAPAROSCOPY INSTRUMENTSMarch 30, 1994
K935950FX-CABLELOK CABLE/PLATE SYSTEMMarch 9, 1994
K932723CONBIO CUB-D10 COPPER LASER SYSTEMFebruary 3, 1994
K930634SUR FLO THERMAL THERAPY PADSNovember 1, 1993
K921056COTREL - DUBOUSSET SPINE IMPLANTSJune 24, 1993
K921767COMPACT COTREL -- DUBOUSSET SPINE SYSTEMJune 22, 1993
K922935CONBIO-MEDLITE Q-SWITCHED ND:YAG LASER SYSTEMApril 7, 1993
K922919DYNACYT BIOPSY ASPIRATION DEVICEMarch 31, 1993