K230817
- 510(k) number
- K230817
- Device name
- TORPEDO Implant System®
- Applicant
- Deltacor GmbH DE
- Product code
- OUR — Sacroiliac Joint Fixation
- Decision date
- 2024-01-19
- Date received
- 2023-03-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K230817.pdf
Official FDA record: K230817
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.