K241990
- 510(k) number
- K241990
- Device name
- SpineSite Endoscope System
- Applicant
- Hydrocision, Inc. MA · US
- Product code
- HRX — Arthroscope
- Decision date
- 2025-07-30
- Date received
- 2024-07-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K241990.pdf
Official FDA record: K241990
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.