The following data is part of a premarket notification filed by Protek, Inc. with the FDA for Schuster Acetabular Cup For Cement/cementless Fix..
| Device ID | K870923 |
| 510k Number | K870923 |
| Device Name: | SCHUSTER ACETABULAR CUP FOR CEMENT/CEMENTLESS FIX. |
| Classification | Prosthesis, Hip, Semi-constrained (metal Uncemented Acetabular Component) |
| Applicant | PROTEK, INC. 5780 WEST 71ST ST. Indianapolis, IN 46278 |
| Contact | Kenneth Epling |
| Correspondent | Kenneth Epling PROTEK, INC. 5780 WEST 71ST ST. Indianapolis, IN 46278 |
| Product Code | KWA |
| CFR Regulation Number | 888.3330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-03-04 |
| Decision Date | 1987-09-14 |