Class Class II

Blueprint Mixed Reality system (K222510)

K222510 2023-01-20 Traditional
Home/ Devices/ Blueprint Mixed Reality system…

Description

Blueprint Mixed Reality system by Tornier S.A.S. — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222510
Clearance Date2023-01-20
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top