# K151379: Conventus PRS System

- Pathway: 510(k) (Traditional)
- Applicant: Conventus Orthopaedics, Inc.
- Decided: Aug 13, 2015 after 83 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: 9 generations back to K962616 (1996). 14 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042135: Synthes (Usa) Elastic Intramedullary Nail (Ein) System (Line Extension), Synthes (Usa) (2004) Summary page 5.
- K102689: Conventus Orthopaedics Fracture Fixation System, Conventus Orthopaedics (2013) Summary page 5.
- K131552: Conventus DRS, Conventus Orthopaedics (2014) Summary page 5.
- (no number) Synthes T-Plate: named in the summary without a submission number

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

## Indications for use
The Conventus PRS™ System is indicated for treatment of proximal radial fractures when internal fixation is desired, and fracture fragments are not too numerous and/or too small to be stabilized with the use of the device.

Source page: https://510kreport.com/device/K151379
Methodology: https://510kreport.com/methodology