510(k) K212739

ActiFlip by Parcus Medical, LLC — Product Code MBI

K212739 is an FDA 510(k) premarket notification submitted by Parcus Medical, LLC for the device "ActiFlip". The FDA issued a decision of Substantially Equivalent on Oct 6, 2021. The device falls under product code MBI (Fastener, Fixation, Nondegradable, Soft Tissue), a Class II device regulated under 21 CFR 888.3040. Parcus Medical, LLC has at least 10 other 510(k) clearances on record.