K253676
- 510(k) number
- K253676
- Device name
- CORUS Posterior Cervical Stabilization System 3D (CORUS PCSS 3D)
- Applicant
- Providence Medical Technology, Inc. CA · US
- Product code
- MRW — System, Facet Screw Spinal Device
- Decision date
- 2026-05-14
- Date received
- 2025-11-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K253676.pdf
Official FDA record: K253676
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.