Class Class II

ArTT Augments and Buttresses and Bone Screws (K251718)

K251718 2025-08-29 Traditional
Home/ Devices/ ArTT Augments and Buttresses…

Description

ArTT Augments and Buttresses and Bone Screws by Lima Corporate S.P.A., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251718
Clearance Date2025-08-29
Clearance TypeTraditional
Product CodeLPH
Regulation Number888.3358

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top