# K110992: Enspire Debrider System

- Pathway: 510(k) (Traditional)
- Applicant: Spine View, Inc.
- Decided: Oct 21, 2011 after 196 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: 6 generations back to K991794 (1999). 26 ancestors in all.
6 later devices descend from it; 3 cite it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K090278: Enspire Debrider System, Spine View, Inc. (2009) Summary page 1.

## Most influential descendants
- K120553: ESPIN (2012), 2 descendants of its own
- K130057: ESPIN (2013), 1 descendant of its own
- K113362: Spinevu Endoscopic Spine System (Sess) (2012), 1 descendant of its own
- K133061: Espin System (2013), 0 descendants of its own
- K121548: Spinevu Endoscopic Spine System (Sess) (2012), 0 descendants of its own

## Indications for use
The enSpire Discectomy System is intended for use in cutting, grinding and aspirating intervertebral disc material during discectomy procedures in the cervical, thoracic and lumbar spine.

Source page: https://510kreport.com/device/K110992
Methodology: https://510kreport.com/methodology