The following data is part of a premarket notification filed by Corin U.s.a. with the FDA for The C-fit & Dc-fit Acetabular Cup System.
| Device ID | K972995 |
| 510k Number | K972995 |
| Device Name: | THE C-FIT & DC-FIT ACETABULAR CUP SYSTEM |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented |
| Applicant | CORIN U.S.A. 10500 UNIVERSITY CENTER DR., SUITE 190 Tampa, FL 33612 |
| Contact | Jack Thomas |
| Correspondent | Jack Thomas CORIN U.S.A. 10500 UNIVERSITY CENTER DR., SUITE 190 Tampa, FL 33612 |
| Product Code | JDI |
| CFR Regulation Number | 888.3350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-08-12 |
| Decision Date | 1997-11-10 |
| Summary: | summary |