# K972704: Kinematic Positioners

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems, Inc.
- Decided: Sep 29, 1997 after 73 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- 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) Signa Profile System (software and electronics): named in the summary without a submission number

## Indications for use
The Indications for Use for the Signa Profile Kinematic Positioner Options expands the capability of the Signa Profile System. The Kinematic Positioner accommodates and improves imaging of the ankle, wrist, cervical-spine and surrounding structures in a dynamic and kinematic motions.

Source page: https://510kreport.com/device/K972704
Methodology: https://510kreport.com/methodology