CORUS Posterior Cervical Stabilization System 3D (CORUS PCSS 3D)— 510(k) K253676
Substantially EquivalentProvidence Medical Technology, Inc.
FDA 510(k) clearance K253676 for CORUS Posterior Cervical Stabilization System 3D (CORUS PCSS 3D), Substantially Equivalent on 2026-05-14. Applicant: Providence Medical Technology, Inc.. Device class: Unclassified.
Summary
Providence Medical Technology's CORUS Posterior Cervical Stabilization System 3D (CORUS PCSS 3D) is filed under MRW, facet screw spinal devices.
Class U, with no regulation number. The classification panel is listed as Unknown, and the Orthopedic review panel handled it as a Traditional 510(k).
Providence filed from Pleasanton, California. Review took 174 calendar days (November 21, 2025 to May 14, 2026).
Clearance details
- Applicant
- Providence Medical Technology, Inc.
- Product code
- Product code MRW
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Pleasanton, CA, US
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