# K022199: Endius Atavi System

- Pathway: 510(k) (Traditional)
- Applicant: Endius, Inc.
- Decided: Oct 2, 2002 after 89 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
Longest line of descent: 1 generation back to K002931 (2000). 1 ancestor in all.
43 later devices descend from it; 2 cite it directly.
0 of 45 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002931: Metrx System, Medtronic Sofamor Danek, Inc. (2000)
- (no number) Sofamor Danek Microendoscopic Discectomy System: named in the summary without a submission number

## Most influential descendants
- K053267: Endius Atavi System (2006), 42 descendants of its own
- K061246: Endoscopic Spine System (2006), 25 descendants of its own
- K061345: Modification to Endius Atavi System (2006), 17 descendants of its own
- K081051: Spinevu Endoscopic Spine System (Sess), Spinevu Miniscope (2008), 16 descendants of its own
- K062038: X-Sten Mild Tool Kit, Model MTK-0001 (2006), 14 descendants of its own

## Indications for use
The Endius@AtaviTMSystem is indicated for use for posterior or anterior access and visualization in the surgical area of the cervical, thoracic, or lumbar spine allowing the surgeon to perform any type of surgical spinal procedures such as discectomy, nucleotomy, spinal fusion, spinal decompression, and insertion of spinal implants. Other examples of generic surgical use of the Endius@AtaviTMSystem would be for use in the knee, ankle, shoulder, hand, wrist, and temporomandibular joint (TMJ).

Source page: https://510kreport.com/device/K022199
Methodology: https://510kreport.com/methodology