FDA 510(k) Application Details - K243697

Device Classification Name System, Image Processing, Radiological

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510(K) Number K243697
Device Name System, Image Processing, Radiological
Applicant Medacta International S.A.
Strada Regina
Castel San Pietro 6874 CH
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Contact Stefano Baj
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Regulation Number 892.2050

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Classification Product Code LLZ
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Date Received 11/29/2024
Decision Date 04/23/2025
Decision SESE - SUBST EQUIV
Classification Advisory Committee RA - Radiology
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review

FDA Source Information for K243697


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