510(k) K910175

FIXATION DEVICES AND BONE PLATE by Micro Surgical Instruments Corp. — Product Code HRS

K910175 is an FDA 510(k) premarket notification submitted by Micro Surgical Instruments Corp. for the device "FIXATION DEVICES AND BONE PLATE". The FDA issued a decision of SN on June 21, 1991. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Micro Surgical Instruments Corp. has at least 10 other 510(k) clearances on record.