The following data is part of a premarket notification filed by T. Koros Surgical Instruments Corp. with the FDA for Microdiscectomy Curette Set.
Device ID | K875292 |
510k Number | K875292 |
Device Name: | MICRODISCECTOMY CURETTE SET |
Classification | Curette, Surgical, General Use |
Applicant | T. KOROS SURGICAL INSTRUMENTS CORP. 610 FLINN AVE. Moorpark, CA 93021 |
Contact | Tibor Koros |
Correspondent | Tibor Koros T. KOROS SURGICAL INSTRUMENTS CORP. 610 FLINN AVE. Moorpark, CA 93021 |
Product Code | FZS |
CFR Regulation Number | 878.4800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-12-30 |
Decision Date | 1988-01-29 |