# K141737: Conventus PHS System

- Pathway: 510(k) (Traditional)
- Applicant: Conventus Orthopaedics, Inc.
- Decided: Apr 8, 2015 after 285 days
- Product code: JDS (Nail, 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). 14 ancestors in all.
No later device cites it as a predicate yet.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K983853: Depuy Ace Timax Meta Plate, Depuy Ace Medical Co. (1998) Summary page 5.
- K033071: Synthes (Usa) Cannulated Titanium Humeral Nail System, Synthes (Usa) (2003) Summary page 5.
- K102689: Conventus Orthopaedics Fracture Fixation System, Conventus Orthopaedics (2013) Summary page 5.

## Indications for use
The Conventus Orthopaedics PHSTM System is indicated for the fixation of proximal humerus fractures except when there are too many fracture fragments to repair the articular surface.

Source page: https://510kreport.com/device/K141737
Methodology: https://510kreport.com/methodology