SpineLinc Anterior Cervical Implant System— 510(k) K250764

Substantially Equivalent

Lincotek Medical

FDA 510(k) clearance K250764 for SpineLinc Anterior Cervical Implant System, Substantially Equivalent on 2025-12-05. Applicant: Lincotek Medical.

Clearance details

Applicant: Lincotek Medical
Product code: Code ODP
Advisory panel: Orthopedic
Date received: 2025-03-13
Decision date: 2025-12-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bartlett, TN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code ODP

product code ODP

Injury: 310
Total: 310

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.