# K953607: Titanium Limited Contact Dynamic Hip Screw Plate (Tilc-DHS)

- Pathway: 510(k) (Traditional)
- Applicant: Synthes (Usa)
- Decided: Mar 8, 1996 after 219 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
No predicates in its family tree.
25 later devices descend from it; 8 cite it directly.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Synthes Dynamic Hip Screw (DHS) Implant: named in the summary without a submission number

## Most influential descendants
- K102057: Targon FN System (2010), 13 descendants of its own
- K152686: Conquest FN (2016), 12 descendants of its own
- K193029: Conquest FN (2020), 10 descendants of its own
- K172785: Conquest FN (2017), 8 descendants of its own
- K210837: Smith & Nephew Plates and Screws (2021), 7 descendants of its own

## Indications for use
Synthes Ti. LC-DHS is a sliding hip screw plate device, 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/K953607
Methodology: https://510kreport.com/methodology