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FDA 510(k) Applications Submitted by Ortoma AB
FDA 510(k) Number
Submission Date
Device Name
Applicant
K250086
01/13/2025
OTS Hip
Ortoma AB
K232140
07/18/2023
OTS Hip
Ortoma AB
K181449
06/01/2018
Ortoma Treatment Solution - OTS
Ortoma AB
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