Johnson & Johnson Professionals, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
206
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K992173SIPHONGUARD CSF CONTROL DEVICEApril 7, 2000
K991413CODMAN ETHISORB DURA PATCHMarch 13, 2000
K991222CODMAN MICROSENSOR VENTRICULAR CATHETER KITJuly 9, 1999
K982379SUNDT SLIM-LINE ANEURYSM CLIP APPLIERDecember 18, 1998
K982812G2 TOTAL HIP SYSTEM FEMORAL STEM (11/13 TAPER)December 4, 1998
K983141CAPITELLO-CONDYLAR TOTAL ELBOW PROSTHESISNovember 6, 1998
K983014SUMMIT ACETABULAR SYSTEMOctober 27, 1998
K980778HAKIM MICRO PROGRAMMABLE VALVE SYSTEMJuly 17, 1998
K974739HAKIM PROGRAMMABLE VALVE SYSTEMJuly 1, 1998
K980801J-FX BIPOLAR HEADMay 29, 1998
K980081S-ROM ZIRCONIA CERAMIC FEMORAL HIP HEADApril 9, 1998
K980286ULTIMA ACETABULAR ROOF REINFORCEMENT RINGApril 3, 1998
K974331UNI-ROM TOTAL HIP SYSTEM FEMORAL STEMFebruary 6, 1998
K974088CODMAN INTRACRANIAL BOLTJanuary 9, 1998
K973774CODMAN HAKIM MICRO PRECISION VALVEDecember 29, 1997
K973307S-ROM ZIRCONIA CERAMIC FEMORAL HIP HEADNovember 20, 1997
K972435ULTIMA AND ULTIMA LX CEMENTED FEMORAL STEMSeptember 11, 1997
K971189P.F.C. SIGMA KNEE SYSTEM (SIZE 1.5)July 17, 1997
K971652P.F.C. SIGMA INSET PATELLAJuly 16, 1997
K971682J-FX CERCLAGE SYSTEMJune 27, 1997