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 |