FDA 510(k) Applications Submitted by Next OrthoSurgical

FDA 510(k) Number Submission Date Device Name Applicant
K161499 06/01/2016 VertiForm Posterior Fixation System NEXT ORTHOSURGICAL
K161608 06/10/2016 InterForm Cervical Interbody Cage System NEXT ORTHOSURGICAL
K141291 05/19/2014 VERTIFORM POSTERIOR FIXATION SYSTEM NEXT ORTHOSURGICAL
K131082 04/18/2013 INTERFORM INTERBODY CAGE SYSTEM NEXT ORTHOSURGICAL
K190981 04/15/2019 NEX-D2 Posterior Fixation System Next OrthoSurgical


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