# K090278: Enspire Debrider System

- Pathway: 510(k) (Traditional)
- Applicant: Spine View, Inc.
- Decided: Apr 15, 2009 after 70 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: 5 generations back to K991794 (1999). 25 ancestors in all.
7 later devices descend from it; 1 cites 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)
- K081051: Spinevu Endoscopic Spine System (Sess), Spinevu Miniscope, Spine View, Inc. (2008) Summary page 1.
- K032473: Dekompressor Percutaneous Discectomy Probe, Stryker Instruments (2003) Summary page 1.

## Most influential descendants
- K110992: Enspire Debrider System (2011), 6 descendants of its own
- 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

## Indications for use
The SpineView ENSPIRE™ Debrider 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/K090278
Methodology: https://510kreport.com/methodology