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FDA 510(k) Applications Submitted by LANTERNA MEDICAL TECHNOLOGIES
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150507
02/26/2015
Santis Pedicle Screw System
LANTERNA MEDICAL TECHNOLOGIES
K133063
09/27/2013
SANTIS PEDICLE SCREW SYSTEM
LANTERNA MEDICAL TECHNOLOGIES
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