# P960025: Brantigen I/F Cage (R) Used with VSP (R) Spine Plates and Pedicle Screws

- Pathway: PMA
- Applicant: Depuy Spine, Inc.
- Decided: Feb 2, 1999 after 922 days
- Product code: MAX (Intervertebral Fusion Device With Bone Graft, Lumbar)
- Device class: 2
- Regulation: 21 CFR 888.3080
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1,714 later devices descend from it; 99 cite it directly.
1 of 1,715 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. PMA decisions do not claim a predicate device.

## Most influential descendants
- K073291: Capstone Spinal System (2008), 1,103 descendants of its own
- K073470: Avs PL Peek Spacers, Models 48351XXX and 48353XXX (2008), 1,102 descendants of its own
- K080758: Avs PL Peek Spacers, Models 48351 and 48353 (2008), 1,091 descendants of its own
- K072791: Oracle Spacer, Opal Spacer (2007), 1,055 descendants of its own
- K100175: Clydesdale Spinal System (2010), 1,008 descendants of its own

Source page: https://510kreport.com/device/P960025
Methodology: https://510kreport.com/methodology