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FDA 510(k) Applications Submitted by JOIMAX GMBH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K151143
04/29/2015
EndoLIF On-Cage
JOIMAX GMBH
K192663
09/25/2019
Joimax Intracs System
joimax GmbH
K192680
09/26/2019
Percusys« Plus Pedicle Screw System
Joimax GmbH
K203014
10/01/2020
EndoLIF Delta-Cage and DoubleWedge-Cage
joimax GmbH
K051827
07/06/2005
JOIMAX ENDOSCOPE/MULTISCOPE, THESSYS FORAMINOSCOPE/MULTISCOPE, THESSYS LAMINOSCOPE/MULTISCOPE
JOIMAX GMBH
K170358
02/06/2017
joimax Endovapor 2
joimax GmbH
K161378
05/18/2016
joimax Electrosurgical Instruments
JOIMAX GMBH
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