meddevicedb.com FDA Device Reference

CORUS™ Posterior Cervical Stabilization System 3D (CORUS™ PCSS 3D)

K253676 Traditional
Decision Date
2026-05-14
Sponsor / Applicant
Providence Medical Technology, Inc.

Technical Specification

510(k) Submission ID K253676
Product Code MRW
Medical Specialty / Panel Unknown
Decision Date 2026-05-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CORUS™ Posterior Cervical Stabilization System 3D (CORUS™ PCSS 3D) received FDA 510(k) clearance under submission number K253676, sponsored by Providence Medical Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Unknown review panel. The statutory decision date of record is 2026-05-14.

Classification & Regulation

This clearance is catalogued under FDA product code MRW , within the Unknown review panel as a device.