K241808
- 510(k) number
- K241808
- Device name
- ApolloHipX (THR.SS.0001)
- Applicant
- Corin U.S.A. Limited FL · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2025-01-07
- Date received
- 2024-06-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.4 MB · U.S. public domain
Also available from FDA: K241808.pdf
Official FDA record: K241808
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.