# K932699: Arthrex AR-8200 Shaver System

- Pathway: 510(k) (Traditional)
- Applicant: Arthrex, Inc.
- Decided: Jan 25, 1994 after 236 days
- Product code: HWE (Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment)
- Device class: 1
- Regulation: 21 CFR 878.4820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K041824: X-Treme Arthroscopic Pump and Shaver System (2005), 6 descendants of its own
- K050580: Smith & Nephew Intelijet Fluid Management Systems (2005), 2 descendants of its own
- K051326: Smith & Nephew 25 Fluid Management System (2005), 1 descendant of its own
- K171794: Smith & Nephew 25 Fluid Management System (2017), 0 descendants of its own
- K131191: 4MM & 5MM Full Radius Blade Plus, 4MM & 5MM Barrel Bur Plus/4MM Barrel Tornado Bur Plus, 4MM & 5MM Aggressive Blade Plus (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K932699
Methodology: https://510kreport.com/methodology