FDA 510(k) Applications Submitted by Mark Wladkowski

FDA 510(k) Number Submission Date Device Name Applicant
K212782 09/01/2021 SternaLock Sternal Closure System Biomet Microfixation
K213072 09/23/2021 2.1 x 255mm Drill, 22mm Stop Biomet Micofixation
K213208 09/29/2021 Twist Drills Biomet Microfixation
K213712 11/24/2021 Pectus Support Bar System Biomet Microfixation


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