510(k) K982735

LIGHT SABER BONE BIOPSY NEEDLE by Minrad, Inc. — Product Code KNW

K982735 is an FDA 510(k) premarket notification submitted by Minrad, Inc. for the device "LIGHT SABER BONE BIOPSY NEEDLE". The FDA issued a decision of Substantially Equivalent on September 9, 1998. 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.