The following data is part of a premarket notification filed by Fci (france Chirurgie Instrumentation) Sas with the FDA for Ezypor.
Device ID | K212741 |
510k Number | K212741 |
Device Name: | EZYPOR |
Classification | Implant, Eye Sphere |
Applicant | FCI (France Chirurgie Instrumentation) SAS 20-22 Rue Louis Armand Paris, FR 75015 |
Contact | Thierry Fetick |
Correspondent | Barbara S. Fant Clinical Research Consultants, Inc. 3308 Jefferson Avenue, Upper Level Cincinnati, OH 45220 |
Product Code | HPZ |
CFR Regulation Number | 886.3320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-08-30 |
Decision Date | 2022-06-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EZYPOR 79234544 5624917 Live/Registered |
FRANCE CHIRURGIE INSTRUMENTATION; SAS 2018-03-15 |