The following data is part of a premarket notification filed by Sulzer Orthopedics, Inc. with the FDA for Precedent Revision Hip System.
| Device ID | K972637 |
| 510k Number | K972637 |
| Device Name: | PRECEDENT REVISION HIP SYSTEM |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented |
| Applicant | SULZER ORTHOPEDICS, INC. 9900 SPECTRUM DR. Austin, TX 78717 |
| Contact | Lori Kleinschrodt Holder |
| Correspondent | Lori Kleinschrodt Holder SULZER ORTHOPEDICS, INC. 9900 SPECTRUM DR. Austin, TX 78717 |
| Product Code | LZO |
| CFR Regulation Number | 888.3353 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-07-15 |
| Decision Date | 1997-10-01 |
| Summary: | summary |