# K991806: VHS Supracondylar Plate System

- Pathway: 510(k) (Traditional)
- Applicant: Walter Abendschein, M.D.
- Decided: Aug 6, 1999 after 72 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.
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) Compression Hip Screw Supracondylar Compression Tube & Plate System (Zimmer): named in the summary without a submission number
- (no number) AMBI Hip Screw System (S &N Richards): named in the summary without a submission number
- (no number) DHS / DCS Dynamic Hip and Condylar Screw System (Synthes): named in the summary without a submission number
- (no number) Versa-Fx Femoral Fixation System (Zimmer): named in the summary without a submission number
- (no number) Omega Plus Supracondylar Sideplates (Howmedica): named in the summary without a submission number
- (no number) Combination NoLok/ Keyed Compression Hip Screw System (DePuy): named in the summary without a submission number
- (no number) Medoff Supracondylar Plate System (Wright Medical Technology): named in the summary without a submission number
- (no number) BMP Supracondylar Cable Plate System (Biomet): named in the summary without a submission number

## Indications for use
The VHS™ Supracondylar Plate System is indicated for use in the treatment of supracondylar fractures and distal femoral fractures.

Source page: https://510kreport.com/device/K991806
Methodology: https://510kreport.com/methodology