Board tracked Radar started tracking this company’s job board (18 open jobs at last check). source ↗
FDA FDA 510(k) clearance: Vital Spinal Fixation System — K253093, Dec 17, 2025. Applicant at approval: Highridge Medical, LLC. source ↗
FDA FDA 510(k) clearance: Virage® OCT Spinal Fixation System — K250332, Apr 4, 2025. Applicant at approval: Highridge Medical, LLC. source ↗
Trial start Not phased (device or behavioral study): Evaluation of Safety and Effectiveness of Primary Hybrid Construct of Mobi-C and ACDF in the Treatment of Two-level Symptomatic Degenerative Disc Disease in the Cervical Spine. source ↗
Upcoming milestones
2029-05 (ESTIMATED) · Not phased · Evaluation of Safety and Effectiveness of Primary Hybrid Construct of Mobi-C and ACDF in the Treatment of Two-level Symptomatic Degenerative Disc Disease in the Cervical Spine. · NCT06485206
Estimated primary completion per ClinicalTrials.gov. Dates move.
Level (Entry/Mid/Senior/Executive) is estimated from the job title and required years of experience. Descriptions are short excerpts (about the first 60 words) of the posting plus skills picked out of it; use Read full posting for the complete text.
Evaluation of Safety and Effectiveness of Primary Hybrid Construct of Mobi-C and ACDF in the Treatment of Two-level Symptomatic Degenerative Disc Disease in the Cervical Spine.
Not phased (device or behavioral study)
Recruiting
Sep 1, 2024
2029-05 (estimated)
FDA records (last 2 years)
FDA 510(k) clearance: Vital Spinal Fixation System — K253093, Dec 17, 2025. Applicant at approval: Highridge Medical, LLC. source ↗
FDA 510(k) clearance: Virage® OCT Spinal Fixation System — K250332, Apr 4, 2025. Applicant at approval: Highridge Medical, LLC. source ↗