# K010179: Ebi Vuecath Spinal Endoscopic System

- Pathway: 510(k) (Special)
- Applicant: Ebi, L.P.
- Decided: Feb 9, 2001 after 21 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K063078: Microendoscope (2006), 2 descendants of its own
- K100533: Vista Endoscope,89 CM, 56CM , Scout Blunt-Tipped Guide- 106 CM, 86 CM, 53 CM, Models FG0027, FG0031, FG0029, FG 0028, (2011), 1 descendant of its own
- K183264: Flex-THOR scope (2019), 0 descendants of its own

## Recalls of this device
- Jun 17, 2003 · Not classified · Z-1006-03: Non sterile device is labeled sterile.

Source page: https://510kreport.com/device/K010179
Methodology: https://510kreport.com/methodology