# K062767: CTL-63 and CTL-128 Spine Array Coils

- Pathway: 510(k) (Special)
- Applicant: Invivo Corporation
- Decided: Oct 13, 2006 after 28 days
- Product code: MOS (Coil, Magnetic Resonance, Specialty)
- 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
To be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic images of the cervical, lumbar, and thoracic regions of the spine that can be interpreted by a trained physician.

Source page: https://510kreport.com/device/K062767
Methodology: https://510kreport.com/methodology