The following data is part of a premarket notification filed by T. Koros Surgical Instruments Corp. with the FDA for Spinal Needle.
| Device ID | K880812 |
| 510k Number | K880812 |
| Device Name: | SPINAL NEEDLE |
| Classification | Needle, Aspiration And Injection, Reusable |
| 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 | GDM |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-02-26 |
| Decision Date | 1988-03-11 |