The following data is part of a premarket notification filed by Monteris Medical with the FDA for Neuroblate System.
| Device ID | K193375 |
| 510k Number | K193375 |
| Device Name: | NeuroBlate System |
| Classification | Powered Laser Surgical Instrument |
| Applicant | Monteris Medical 14755 27th Avenue North; Suite C Plymouth, MN 55447 |
| Contact | David H. Mueller |
| Correspondent | David H. Mueller Monteris Medical 14755 27th Avenue North; Suite C Plymouth, MN 55447 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-12-05 |
| Decision Date | 2020-01-03 |