# K120680: Enspire Discectomy System

- Pathway: 510(k) (Special)
- Applicant: Spine View, Inc.
- Decided: Jun 26, 2012 after 112 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: 7 generations back to K991794 (1999). 27 ancestors in all.
No later device cites it as a predicate yet.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110992: Enspire Debrider System, Spine View, Inc. (2011) Summary page 1.

## Indications for use
The enSpire Tm 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/K120680
Methodology: https://510kreport.com/methodology