K242272
- 510(k) number
- K242272
- Device name
- CORIOGRAPH Pre-Op Planning and Modeling Services
- Applicant
- Blue Belt Technologies, Inc. PA · US
- Decision date
- 2024-11-15
- Date received
- 2024-08-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
510(k) Summary (official FDA PDF): K242272.pdf
Official FDA record: K242272
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.