# K113362: Spinevu Endoscopic Spine System (Sess)

- Pathway: 510(k) (Special)
- Applicant: Spine View, Inc.
- Decided: Feb 10, 2012 after 87 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). 31 ancestors in all.
1 later device descends 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.
- K110992: Enspire Debrider System, Spine View, Inc. (2011) Summary page 1.
- K061345: Modification to Endius Atavi System, Endius, Inc. (2006) Summary page 1.
- K994363: Instruments for Minimally Invasive Spinal Surgery (Miss), Richard Wolf Medical Instruments Corp. (2000) Summary page 1.
- K001918: Ksea Percutaneous Foraminoscopy Set, KARL STORZ Endoscopy-America, Inc. (2000) Summary page 1.

## Most influential descendants
- K121548: Spinevu Endoscopic Spine System (Sess) (2012), 0 descendants of its own

## Indications for use
surgical accessories are indicated for facilitating endoscopic access and visualization in the surgical area of the cervical, thoracic, or lumbar spine for interventional spinal procedures such as discectomy, nucleotomy and foraminotomy.

Source page: https://510kreport.com/device/K113362
Methodology: https://510kreport.com/methodology