# K082194: Laurimed Percutaneous Discectomy System, Model FG-000002

- Pathway: 510(k) (Traditional)
- Applicant: Laurimed, LLC
- Decided: Aug 28, 2008 after 24 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: 1 generation back to K914282 (1991). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K923525: Nucleotome 3.5 MM Automated Percutaneous Lumbar, Surgical Dynamics, Inc. (1993) Summary page 1.
- K914282: Nucleotome (R) II (VERSION2) Tissue Aspira/Cutter, Surgical Dynamics, Inc. (1991) Summary page 1.

## Most influential descendants
- K090815: Percutaneous Discectomy System (2009), 0 descendants of its own

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

Source page: https://510kreport.com/device/K082194
Methodology: https://510kreport.com/methodology