# K131552: Conventus DRS

- Pathway: 510(k) (Traditional)
- Applicant: Conventus Orthopaedics
- Decided: Feb 12, 2014 after 258 days
- Product code: HRS (Plate, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K962616 (1996). 12 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102689: Conventus Orthopaedics Fracture Fixation System, Conventus Orthopaedics (2013) Summary page 1.

## Most influential descendants
- K151379: Conventus PRS System (2015), 1 descendant of its own
- K161048: Conventus Orthopaedics Ulna Fixation System (2016), 0 descendants of its own

## Indications for use
The Conventus DRSTM is intended for the fixation of distal radius fractures.

Source page: https://510kreport.com/device/K131552
Methodology: https://510kreport.com/methodology