# K023851: Precimed Hip Screw System

- Pathway: 510(k) (Traditional)
- Applicant: Precimed, Inc.
- Decided: Jan 28, 2003 after 70 days
- Product code: KTT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component)
- 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.
5 later devices descend from it; 1 cites it directly.
0 of 6 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) AMBI Hip Screw System (S &N Richards): named in the summary without a submission number
- (no number) HDS / DCS Dynamic Hip & Condylar Screw System (Synthes): named in the summary without a submission number
- (no number) Syntec-Taichung DHS / DCS Plate System (Syntec-Taichung Medical Instrument Co.): named in the summary without a submission number

## Most influential descendants
- K071852: Aap Aps System (2007), 4 descendants of its own
- K120360: Ortho Solutions Trauma Plates for Osteosysnthesis (2012), 2 descendants of its own
- K202764: Ortho Solutions Plating System (2020), 1 descendant of its own
- K221787: Auxein's DHS/DCS Plate System (2023), 0 descendants of its own
- K210658: Volition Plating System (2021), 0 descendants of its own

## Indications for use
The Precimed Hip Screw System is indicated for use in the treatment of dis-placed sub-capital fractures, subtrochanteric and intertrochanteric fractures, arthrodesis, moderately displaced femoral capital epiphysis, varus or valgus osteotomies of the hip, medial displacement osteotomies, supracondylar and distal femur fractures.

Source page: https://510kreport.com/device/K023851
Methodology: https://510kreport.com/methodology