# K011454: Spine Scope, Model 2180

- Pathway: 510(k) (Traditional)
- Applicant: Clarus Medical, LLC
- Decided: Dec 13, 2001 after 216 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.
40 later devices descend from it; 3 cite it directly.
0 of 41 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
- K082841: Spinal Foraminoscope (2009), 20 descendants of its own
- K040424: Laser Endoscopic Decompression Kit, Model 1100, and Percutaneous Discectomy Kit, Model 1120 (2004), 18 descendants of its own
- K040919: Nucleotome Probe Set, Model 21200 (2004), 17 descendants of its own
- K130778: Discoscopes, Cervical Endoscopes (2014), 14 descendants of its own
- K062038: X-Sten Mild Tool Kit, Model MTK-0001 (2006), 14 descendants of its own

Source page: https://510kreport.com/device/K011454
Methodology: https://510kreport.com/methodology