# K071814: Light Sabre Spinal Access Device

- Pathway: 510(k) (Traditional)
- Applicant: Minrad, Inc.
- Decided: Oct 16, 2007 after 106 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
Longest line of descent: 1 generation back to K982735 (1998). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982735: Light Saber Bone Biopsy Needle, Minrad, Inc. (1998) Summary page 1.

## Indications for use
The Light SabreTM Spinal Access Device is a single-use disposable device that is used to obtain biopsies of bone and/or bone marrow and is used to provide a port of entry to place guidewires during percutaneous spinal procedures.

Source page: https://510kreport.com/device/K071814
Methodology: https://510kreport.com/methodology