FDA 510(k) Application Details - K233639

Device Classification Name Marker, Radiographic, Implantable

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510(K) Number K233639
Device Name Marker, Radiographic, Implantable
Applicant Elucent Medical, Inc.
6509 Flying Cloud Drive
Eden Prairie, MN 55344 US
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Contact Judson Guericke
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Regulation Number 878.4300

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Classification Product Code NEU
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Date Received 11/13/2023
Decision Date 12/20/2024
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review

FDA Source Information for K233639


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