The following data is part of a premarket notification filed by Elliquence Llc with the FDA for Disc-fx System.
| Device ID | K162490 |
| 510k Number | K162490 |
| Device Name: | Disc-FX System |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | ELLIQUENCE LLC 2455 Grand Avenue Baldwin, NY 11510 |
| Contact | Paul D. Buhrke Iv |
| Correspondent | Paul D. Buhrke Iv ELLIQUENCE LLC 2455 Grand Avenue Baldwin, NY 11510 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-09-07 |
| Decision Date | 2017-01-06 |
| Summary: | summary |