# K142534: HyProCure II

- Pathway: 510(k) (Traditional)
- Applicant: Graham Medical Technologies, LLC Dba Gramedica
- Decided: Oct 3, 2014 after 24 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- 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 K042030 (2004). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042030: Hyprocure Subtalar Implant System, Graham Medical Technologies, LLC (2004) Summary page 4.

## Most influential descendants
- K251382: Phoenix Sinus Tarsi Stent System (2025), 0 descendants of its own
- K170624: TalarLift STS (2017), 0 descendants of its own

## Indications for use
HyProCure II (HYP II and HYP IIs) is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion.

Source page: https://510kreport.com/device/K142534
Methodology: https://510kreport.com/methodology