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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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