Class Class II

360CAS (K223927)

K223927 2023-01-27 Special
Home/ Devices/ 360CAS (K223927)

Description

360CAS by Kico Knee Innovation Company Pty Limited — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223927
Clearance Date2023-01-27
Clearance TypeSpecial
Product CodeOLO
Regulation Number882.4560

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top