Sulzer Orthopedics, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 45
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K022985 | ASCENDENT ACETABULAR SYSTEM | December 5, 2002 |
| K021578 | NATURAL-KNEE II SYSTEM COCR TIBIAL BASEPLATE | August 9, 2002 |
| K020713 | MS-30 LATERAL FEMORAL STEM | May 14, 2002 |
| K013935 | ALLOFIT ACETABULAR SYSTEM 32MM ALPHA DURASUL INSERTS | December 13, 2001 |
| K013031 | MOST OPTIONS SYSTEM | December 7, 2001 |
| K012739 | CONVERGE ACETABULAR SYSTEM | November 14, 2001 |
| K012961 | SULZER ORTHOPEDICS CONVERGE ACETABULAR SYSTEM | October 18, 2001 |
| K011954 | SULZER ORTHOPEDICS ALLEGRETTO UNICOMPARTMENTAL KNEE | September 19, 2001 |
| K010839 | CLS VARUS STEM/CLS 135 STEM | April 18, 2001 |
| K003758 | ALLOFIT ACETABULAR SYSTEM | March 7, 2001 |
| K003801 | ANATOMICAL PRESS-FIT HUMERAL STEM | February 28, 2001 |
| K003832 | SULZER ORTHOPEDICS ANATOMICAL SHOULDER CEMENTED HUMERAL STEM | January 4, 2001 |
| K003269 | UNICONDYLAR INTERPOSITIONAL SPACER | January 4, 2001 |
| K002575 | INTER-OP DURASUL ACETABULAR INSERTS (4MM) | November 15, 2000 |
| K002356 | NATURAL-KNEE II PATELLOFEMORAL JOINT PROSTHESIS | October 30, 2000 |
| K002335 | NATURAL-KNEE II SYSTEM-DURASUL TIBIAL INSERT AND DURASUL ALL-POLY PATELLA | October 25, 2000 |
| K001536 | INTER-OP METASUL HOODED AND PROTRUSIO ACETABULAR INSERTS | July 27, 2000 |
| K001320 | SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM | July 7, 2000 |
| K001078 | SULZER ORTHOPEDICS MS-30 FEMORAL STEM | June 23, 2000 |
| K993259 | INTER-OP DURASUL ACETABULAR INSERTS/COCR FEMORAL HEADS | March 10, 2000 |