The following data is part of a premarket notification filed by Gt Medical Technologies with the FDA for Gammatile.
| Device ID | K190296 |
| 510k Number | K190296 |
| Device Name: | GammaTile |
| Classification | Source, Brachytherapy, Radionuclide |
| Applicant | GT Medical Technologies 1809 S Holbrook Drive, Suite 107 Tempe, AZ 85281 |
| Contact | Jessica Newhard |
| Correspondent | Jessica Newhard GT Medical Technologies 1809 S Holbrook Drive, Suite 107 Tempe, AZ 85281 |
| Product Code | KXK |
| CFR Regulation Number | 892.5730 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-02-11 |
| Decision Date | 2019-03-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() GAMMATILE 88226299 not registered Live/Pending |
GT MEDICAL TECHNOLOGIES, INC. 2018-12-12 |
![]() GAMMATILE 86570994 not registered Dead/Abandoned |
GT MEDICAL TECHNOLOGIES, INC. 2015-03-20 |