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FDA 510(k) Application Details - K233639
Device Classification Name
Marker, Radiographic, Implantable
More FDA Info for this Device
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
Other 510(k) Applications for this Contact
Regulation Number
878.4300
More FDA Info for this Regulation Number
Classification Product Code
NEU
Other 510(k) Applications for this Device
More FDA Info for this Product Code
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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