Sulzer Orthopedics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
45
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K022985ASCENDENT ACETABULAR SYSTEMDecember 5, 2002
K021578NATURAL-KNEE II SYSTEM COCR TIBIAL BASEPLATEAugust 9, 2002
K020713MS-30 LATERAL FEMORAL STEMMay 14, 2002
K013935ALLOFIT ACETABULAR SYSTEM 32MM ALPHA DURASUL INSERTSDecember 13, 2001
K013031MOST OPTIONS SYSTEMDecember 7, 2001
K012739CONVERGE ACETABULAR SYSTEMNovember 14, 2001
K012961SULZER ORTHOPEDICS CONVERGE ACETABULAR SYSTEMOctober 18, 2001
K011954SULZER ORTHOPEDICS ALLEGRETTO UNICOMPARTMENTAL KNEESeptember 19, 2001
K010839CLS VARUS STEM/CLS 135 STEMApril 18, 2001
K003758ALLOFIT ACETABULAR SYSTEMMarch 7, 2001
K003801ANATOMICAL PRESS-FIT HUMERAL STEMFebruary 28, 2001
K003832SULZER ORTHOPEDICS ANATOMICAL SHOULDER CEMENTED HUMERAL STEMJanuary 4, 2001
K003269UNICONDYLAR INTERPOSITIONAL SPACERJanuary 4, 2001
K002575INTER-OP DURASUL ACETABULAR INSERTS (4MM)November 15, 2000
K002356NATURAL-KNEE II PATELLOFEMORAL JOINT PROSTHESISOctober 30, 2000
K002335NATURAL-KNEE II SYSTEM-DURASUL TIBIAL INSERT AND DURASUL ALL-POLY PATELLAOctober 25, 2000
K001536INTER-OP METASUL HOODED AND PROTRUSIO ACETABULAR INSERTSJuly 27, 2000
K001320SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEMJuly 7, 2000
K001078SULZER ORTHOPEDICS MS-30 FEMORAL STEMJune 23, 2000
K993259INTER-OP DURASUL ACETABULAR INSERTS/COCR FEMORAL HEADSMarch 10, 2000