# K081446: BD Spinal Needle, Models: 405081, 405235, 405236, 405237

- Pathway: 510(k) (Abbreviated)
- Applicant: Becton, Dickinson & CO
- Decided: Jul 17, 2008 after 56 days
- Product code: BSP (Needle, Conduction, Anesthetic (W/Wo Introducer))
- Device class: 2
- Regulation: 21 CFR 868.5150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) BD Spinal Needle: named in the summary without a submission number
- (no number) BD Precisionglide Needle: named in the summary without a submission number
- (no number) BD Hypoint Needle: named in the summary without a submission number

## Indications for use
An anesthesia conduction needle is a device used to inject local anesthetics into a patient to provide regional anesthesia.

Source page: https://510kreport.com/device/K081446
Methodology: https://510kreport.com/methodology