# K955348: Titanium Moss Miami Spinal System

- Pathway: 510(k) (Traditional)
- Applicant: Depuy, Inc.
- Decided: Feb 16, 1996 after 87 days
- Product code: KWP (Appliance, Fixation, Spinal Interlaminal)
- Device class: 2
- Regulation: 21 CFR 888.3050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1,019 later devices descend from it; 34 cite it directly.
1 of 1,020 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
- K964024: Depuy Motech Titanium Moss Miami Spinal System (1997), 700 descendants of its own
- K010576: Monarch Spine System (2001), 596 descendants of its own
- K024348: Monarch Spine System (2003), 578 descendants of its own
- K062196: SFX Snap-Fit Cross Connector (2006), 559 descendants of its own
- K992168: Moss Miami 6.35MM Polyaxial Screw (1999), 547 descendants of its own

Source page: https://510kreport.com/device/K955348
Methodology: https://510kreport.com/methodology