Class Class II

All-Suture Dual Anchor System (K250095)

K250095 2025-09-05 Traditional
Home/ Devices/ All-Suture Dual Anchor System…

Description

All-Suture Dual Anchor System by Suturetech, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250095
Clearance Date2025-09-05
Clearance TypeTraditional
Product CodeMBI
Regulation Number888.3040

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top