# K080122: Sopro 670 Arthroscopic Pump

- Pathway: 510(k) (Traditional)
- Applicant: Sopro
- Decided: Jul 11, 2008 after 176 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 K954465 (1995). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K954465: FMS Duo, Future Medical Systems, Inc. (1995) Summary page 1.

## Indications for use
The SOPRO 670 irrigation pump is a arthroscopic pump system intended to provide fluid distension and irrigation of knee, shoulder, hip, elbow, ankle and wrist joint cavities and fluid suction during diagnostic and operative arthroscopic procedures that may only be used by qualified physicians

Source page: https://510kreport.com/device/K080122
Methodology: https://510kreport.com/methodology