# K152511: Neo - Arthroscope (Rigid) 2.0mm/3.5mm, Outer sheath/ cannula, Outer sheath/ cannula w/ Handle, Trocar for outersheath/ cannula

- Pathway: 510(k) (Traditional)
- Applicant: Prosurg, Inc.
- Decided: Jul 11, 2016 after 313 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: 6 generations back to K833587 (1983). 18 ancestors in all.
No later device cites it as a predicate yet.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K140903: Nuvis Arthroscope, Integrated Endoscopy, Inc. (2014) Summary page 4.

## Indications for use
The Prosurg’s Neo-Arthroscope ™ -Digital Video Arthroscopic System (which includes Digital Video Arthroscope, Single use Outer Sheath is intended to provide an internal view or image of the interior of a joint through surgical opening during examination, diagnostic / operating, arthroscopic / endoscopic treatment procedures including examination, diagnostic & surgical procedures for treatment of knee, shoulder. ankle, elbow, Hip, wrist (Carpel Tunnel Syndrome). hand, TMJ (Temporal Mandibular Joint), Spine, Disc and feet (Planter fascia Release) using surgical devices and accessorics.

Source page: https://510kreport.com/device/K152511
Methodology: https://510kreport.com/methodology