# K210247: OsteoCentric Integrated Hip Fastener System

- Pathway: 510(k) (Traditional)
- Applicant: Osteocentric Technologies D.B.A. Osteocentric Trauma
- Decided: Apr 30, 2021 after 91 days
- Product code: JDO (Device, Fixation, Proximal Femoral, Implant)
- 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: 12 generations back to K962616 (1996). 97 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 99 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K953607: Titanium Limited Contact Dynamic Hip Screw Plate (Tilc-DHS), Synthes (Usa) (1996) Summary page 5.
- K923613: Synthes Limited Contact-Dynamic Hip Screw Implant, Synthes (Usa) (1993) Summary page 5.
- K791619: Dynamic Hip Screw, Synthes (Usa) (1979) Summary page 5.
- K914546: Angled Blade Plate, Synthes (Usa) (1991) Summary page 5.
- K193029: Conquest FN, Smith & Nephew, Inc. (2020) Summary page 5.
- K150818: Versa-Fx Femoral Fixation System, Versa-Fx II Femoral Fixation System, Free-Lock Femoral Fixation System, Zimmer, Inc. (2015) Summary page 5.
- K000972: Synthes (Usa) Trochanter Stabilization Plate for DHS, Synthes (Usa) (2000) Summary page 5.
- K120772: NCB Periprosthetic Trochanter Plates and Screws, NCB Cable Button for NCB Oplyaxial Locking Plate, Zimmer GmbH (2012) Summary page 5.

## Most influential descendants
- K230764: OsteoCentric Integrated Hip Fastener System (2023), 0 descendants of its own

## Indications for use
The OsteoCentric Integrated Hip Fastener System is intended to treat stable and unstable intertrochanteric, subtrochanteric, and basilar neck fractures in which a stable medial buttress can be reconstructed.

Source page: https://510kreport.com/device/K210247
Methodology: https://510kreport.com/methodology