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FDA 510(k) Applications Submitted by SPINEOLOGY INC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160980
04/07/2016
Threshold Pedicular Fixation System, Palisade Pedicular Fixation System
SPINEOLOGY INC
K182322
08/27/2018
Duo Lumbar Interbody Fusion Device
Spineology Inc
K182345
08/28/2018
Spineology Navigation Instruments
Spineology Inc
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