COMPANY
MiRus
Timeline
- FDA FDA 510(k) clearance: EUROPA Posterior Cervical Fusion Navigated Instruments — K253444, Mar 18, 2026. Applicant at approval: MiRus, LLC. source ↗
- FDA FDA 510(k) clearance: ATLAS Expandable Osteotomy Wedge System — K252733, Feb 19, 2026. Applicant at approval: MiRus, LLC. source ↗
- FDA FDA 510(k) clearance: EUROPA Posterior Cervical Fusion System — K242516, Nov 19, 2024. Applicant at approval: MiRus, LLC. source ↗
FDA records (last 2 years)
- FDA 510(k) clearance: EUROPA Posterior Cervical Fusion Navigated Instruments — K253444, Mar 18, 2026. Applicant at approval: MiRus, LLC. source ↗
- FDA 510(k) clearance: ATLAS Expandable Osteotomy Wedge System — K252733, Feb 19, 2026. Applicant at approval: MiRus, LLC. source ↗
- FDA 510(k) clearance: EUROPA Posterior Cervical Fusion System — K242516, Nov 19, 2024. Applicant at approval: MiRus, LLC. source ↗
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