Class Class II

SutureLoc™ Implant (K223284)

K223284 2023-02-02 Traditional
Home/ Devices/ SutureLoc™ Implant (K223284)

Description

SutureLoc™ Implant by Arthrex, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223284
Clearance Date2023-02-02
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