510(k) K090669

RIGIDFIX BIOCRYL CROSS PIN KITS by Depuy Mitek, A Johnson & Johnson Company — Product Code MAI

K090669 is an FDA 510(k) premarket notification submitted by Depuy Mitek, A Johnson & Johnson Company for the device "RIGIDFIX BIOCRYL CROSS PIN KITS". The FDA issued a decision of Substantially Equivalent on Apr 3, 2009. The device falls under product code MAI (Fastener, Fixation, Biodegradable, Soft Tissue), a Class II device regulated under 21 CFR 888.3030. Depuy Mitek, A Johnson & Johnson Company has 61 other 510(k) clearances on record.