# K090815: Percutaneous Discectomy System

- Pathway: 510(k) (Traditional)
- Applicant: Laurimed, LLC
- Decided: May 21, 2009 after 57 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: 2 generations back to K914282 (1991). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082194: Laurimed Percutaneous Discectomy System, Model FG-000002, Laurimed, LLC (2008) Summary page 1.

## Indications for use
The Laurimed Discectomy System is indicated for use in aspiration of disc material during open discectomies in the lumbar region of the spine.

Source page: https://510kreport.com/device/K090815
Methodology: https://510kreport.com/methodology