510(k) K070780

CONMED LINVATEC XO BUTTON by Conmed Linvatec — Product Code MBI

K070780 is an FDA 510(k) premarket notification submitted by Conmed Linvatec for the device "CONMED LINVATEC XO BUTTON". The FDA issued a decision of Substantially Equivalent on Aug 21, 2007. The device falls under product code MBI (Fastener, Fixation, Nondegradable, Soft Tissue), a Class II device regulated under 21 CFR 888.3040. Conmed Linvatec has at least 10 other 510(k) clearances on record.