# K950697: Depuy Motech Moss Miami Spinal System - Pedicle Fixation

- Pathway: 510(k) (Traditional)
- Applicant: Depuy Motech
- Decided: Jun 22, 1995 after 136 days
- Product code: MNH (Orthosis, Spondylolisthesis Spinal Fixation)
- Device class: 2
- Regulation: 21 CFR 888.3070
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
849 later devices descend from it; 16 cite it directly.
1 of 850 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K050461: Xia 4.5 Spinal System (2005), 742 descendants of its own
- K052761: Modification to:  Xia 4.5 Spinal System (2005), 735 descendants of its own
- K060361: Xia Spinal System, Xia 4.5 Spinal System (2006), 734 descendants of its own
- K060979: Xia Titanium and 4.5 Spinal Systems (2006), 710 descendants of its own
- K082942: Modfication to: Expedium Spine System (2008), 518 descendants of its own

Source page: https://510kreport.com/device/K950697
Methodology: https://510kreport.com/methodology