The following data is part of a premarket notification filed by Sulzer Orthopedics, Inc. with the FDA for Inter-op Metasul Acetabular System.
Device ID | K974728 |
510k Number | K974728 |
Device Name: | INTER-OP METASUL ACETABULAR SYSTEM |
Classification | Prosthesis, Hip, Semi-constrained (metal Uncemented Acetabular Component) |
Applicant | SULZER ORTHOPEDICS, INC. 9900 SPECTRUM DR. Austin, TX 78717 |
Contact | Mitchell A Dhority |
Correspondent | Mitchell A Dhority SULZER ORTHOPEDICS, INC. 9900 SPECTRUM DR. Austin, TX 78717 |
Product Code | KWA |
CFR Regulation Number | 888.3330 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-12-18 |
Decision Date | 1999-08-03 |
Summary: | summary |