# K130242: Maven Pro

- Pathway: 510(k) (Traditional)
- Applicant: Nsequence
- Decided: Aug 29, 2013 after 210 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K954678 (1996). 13 ancestors in all.
No later device cites it as a predicate yet.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070803: Invivodental, Anatomage, Inc. (2007) Summary page 1.

## Indications for use
Maven Pro is intended for use as a front-end software interface for the transfer of imaging information from a medical scanner such as a Dental CT scanner. It Is also Intended for use as a planning and simulation software In the placement of dental Implants and surgical treatment,

Source page: https://510kreport.com/device/K130242
Methodology: https://510kreport.com/methodology