510(k) K161896

Biomet Microfixation Sternal Closure System by Biomet Microfixation — Product Code HRS

K161896 is an FDA 510(k) premarket notification submitted by Biomet Microfixation for the device "Biomet Microfixation Sternal Closure System". The FDA issued a decision of Substantially Equivalent on August 2, 2016. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Biomet Microfixation has at least 10 other 510(k) clearances on record.