K242271
- 510(k) number
- K242271
- Device name
- Caduceus S
- Applicant
- Taiwan Main Orthopaedic Biotechnology Co., Ltd. TW
- Product code
- SBF — Orthopedic Augmented Reality
- Decision date
- 2024-10-30
- Date received
- 2024-08-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K242271.pdf
Official FDA record: K242271
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.