# K210741: KLS Martin Neuro Rongeurs

- Pathway: 510(k) (Traditional)
- Applicant: KLS-Martin L.P.
- Decided: Jun 3, 2022 after 448 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: 3 generations back to K943635 (1994). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K150468: Laminectomy Rongeurs, Kerrison Rongeurs, IVD Rongeurs, K2 Medical GmbH & Co. KG (2016) Summary page 4.

## Indications for use
KLS Martin Neuro Rongeurs are manually operated instruments indicated for cutting or biting bone during surgery involving the skull or spinal column in patients two years of age or older.

Source page: https://510kreport.com/device/K210741
Methodology: https://510kreport.com/methodology