K232350
- 510(k) number
- K232350
- Device name
- Stryker Facial iD System
- Applicant
- Stryker Craniomaxillofacial MI · US
- Product code
- JEY — Plate, Bone
- Decision date
- 2024-01-13
- Date received
- 2023-08-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232350.pdf
Official FDA record: K232350
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.