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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