# K982390: Concise Compression Hip Screw System (Sterile)

- Pathway: 510(k) (Traditional)
- Applicant: Wrightmedicaltechnologyinc
- Decided: Sep 14, 1998 after 67 days
- Product code: KTW (Appliance, Fixation, Nail/Blade/Plate Combination, Single 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.
No later device cites it as a predicate yet.
0 of 1 device 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) CONCISE Compression Hip Screw System (Non-Sterile): named in the summary without a submission number

## Indications for use
The CONCISE™ Compression Hip Screw System is indicated for stable and unstable fractures in which a stable medial buttress can be reconstructed for fractures of the proximal femur including: . Intertrochanteric fractures . Subtrochanteric fractures . Basilar neck fractures . Selected trochanteric non-unions

Source page: https://510kreport.com/device/K982390
Methodology: https://510kreport.com/methodology