The following data is part of a premarket notification filed by Sulzer Orthopedics, Inc. with the FDA for Anatomica Glenoid Component.
| Device ID | K990136 |
| 510k Number | K990136 |
| Device Name: | ANATOMICA GLENOID COMPONENT |
| Classification | Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented |
| 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 | KWS |
| CFR Regulation Number | 888.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-01-14 |
| Decision Date | 1999-03-01 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00889024285873 | K990136 | 000 |
| 00889024285859 | K990136 | 000 |
| 00889024285835 | K990136 | 000 |