# P050010: Prodisc -L Total Disc Replacement Device

- Pathway: PMA
- Applicant: Centinel Spine, LLC
- Decided: Aug 14, 2006 after 517 days
- Product code: MJO (Prosthesis, Intervertebral Disc)
- Device class: 3
- 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. PMA decisions do not claim a predicate device.

Source page: https://510kreport.com/device/P050010
Methodology: https://510kreport.com/methodology