510(k) K071814

LIGHT SABRE SPINAL ACCESS DEVICE by Minrad, Inc. — Product Code KNW

K071814 is an FDA 510(k) premarket notification submitted by Minrad, Inc. for the device "LIGHT SABRE SPINAL ACCESS DEVICE". The FDA issued a decision of Substantially Equivalent on October 16, 2007. The device falls under product code KNW (Instrument, Biopsy), a Class II device regulated under 21 CFR 876.1075. Minrad, Inc. has at least 10 other 510(k) clearances on record.