# K953915: Moss Miami Spinal System (Anterior Use)

- Pathway: 510(k) (Traditional)
- Applicant: Depuy, Inc.
- Decided: Feb 15, 1996 after 178 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.
765 later devices descend from it; 8 cite it directly.
1 of 766 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
- K012916: Frontier Anterior Scoliosis System (2001), 601 descendants of its own
- K071668: Orthobiom Spinal System (2008), 582 descendants of its own
- K091445: CD Horizon Spinal System (2010), 581 descendants of its own
- K982511: Depuy Motech Moss Miami Spinal Systems (1998), 413 descendants of its own
- K030383: Modification to Moss Miami Spinal System Polyaxial Screws (2003), 410 descendants of its own

Source page: https://510kreport.com/device/K953915
Methodology: https://510kreport.com/methodology