# K090132: Maxmorespine Spinal System

- Pathway: 510(k) (Abbreviated)
- Applicant: Hoogland Spine Products, GmbH
- Decided: Jun 9, 2009 after 139 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: 4 generations back to K991794 (1999). 12 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051827: Joimax Endoscope/Multiscope, Thessys Foraminoscope/Multiscope, Thessys Laminoscope/Multiscope, Joimax GmbH (2005)
- K973405: Yeung Endoscopic Spine System, Richard Wolf Medical Instruments Corp. (1998) Summary page 2.
- K061246: Endoscopic Spine System, Arthro Kinetics, Inc. (2006) Summary page 2.

## Most influential descendants
- K121482: Instrument System for Endoscopic Spinal Surgery (2012), 0 descendants of its own

## Indications for use
The maxMorespine System is intended to visualize the inside of the patient through a cannulated incision for diagnostic and surgical procedures such as; arthroplasty, nucleotomy, discqectomy and foraminotomy.

Source page: https://510kreport.com/device/K090132
Methodology: https://510kreport.com/methodology