# K023187: Ksea Spinoscope

- Pathway: 510(k) (Traditional)
- Applicant: Karl Storz Endoscopy
- Decided: Dec 2, 2002 after 69 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
The Spinoscope is intended for use to view and facilitate treatment of disc herniations in the lumbar region of the spine (including disc prolapses and foramen stenoses).

Source page: https://510kreport.com/device/K023187
Methodology: https://510kreport.com/methodology