The following data is part of a premarket notification filed by T. Koros Surgical Instruments Corp. with the FDA for Cervical Self-retaining Retractor.
Device ID | K935529 |
510k Number | K935529 |
Device Name: | CERVICAL SELF-RETAINING RETRACTOR |
Classification | Retractor, Self-retaining, For Neurosurgery |
Applicant | T. KOROS SURGICAL INSTRUMENTS CORP. 610 FLINN AVE. Moorpark, CA 93021 |
Contact | Roy A Havens |
Correspondent | Roy A Havens T. KOROS SURGICAL INSTRUMENTS CORP. 610 FLINN AVE. Moorpark, CA 93021 |
Product Code | GZT |
CFR Regulation Number | 882.4800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-11-16 |
Decision Date | 1994-03-22 |