The following data is part of a premarket notification filed by Brainlab Ag with the FDA for Exactrac Dynamic.
Device ID | K211939 |
510k Number | K211939 |
Device Name: | ExacTrac Dynamic |
Classification | Accelerator, Linear, Medical |
Applicant | Brainlab AG Olof-Palme-Str. 9 Munich, DE 81829 |
Contact | Chiara Cunico |
Correspondent | Chiara Cunico Brainlab AG Olof-Palme-Str. 9 Munich, DE 81829 |
Product Code | IYE |
CFR Regulation Number | 892.5050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-06-23 |
Decision Date | 2021-07-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EXACTRAC DYNAMIC 79224882 5630026 Live/Registered |
Brainlab AG 2017-11-07 |