# K230256: Rebellion, Phantom Multi-Bite Kerrison Rongeur

- Pathway: 510(k) (Special)
- Applicant: Morpheus AG
- Decided: Mar 3, 2023 after 31 days
- Product code: HAE (Rongeur, Manual)
- Device class: 2
- Regulation: 21 CFR 882.4840
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K902819 (1990). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K200768: Rebellion, Phantom Multi-Bite Kerrison Rongeur, Morpheus AG (2021) Summary page 5.
- K221818: Rebellion; Phantom Multi-Bite Kerrison Rongeur, Morpheus AG (2022) Summary page 5.

## Indications for use
The Rebellion is intended for cutting and removing bone, vertebral bodies and tissue in orthopedics, neurosurgery and spine surgery involving the skull or spinal column.

Source page: https://510kreport.com/device/K230256
Methodology: https://510kreport.com/methodology