# K982735: Light Saber Bone Biopsy Needle

- Pathway: 510(k) (Traditional)
- Applicant: Minrad, Inc.
- Decided: Sep 9, 1998 after 35 days
- Product code: KNW (Instrument, Biopsy)
- Device class: 2
- Regulation: 21 CFR 876.1075
- 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 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K071814: Light Sabre Spinal Access Device (2007), 0 descendants of its own

## Indications for use
Disposable needle for obtaining biopsies from Bone and Bone Marrow.

Source page: https://510kreport.com/device/K982735
Methodology: https://510kreport.com/methodology