# K990519: Phoenix Epidural & Spinal Needles

- Pathway: 510(k) (Traditional)
- Applicant: Myco Medical Supplies, Inc.
- Decided: Jun 2, 2000 after 470 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.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K183316: Dr J Spinal and Epidural Needles (2019), 1 descendant of its own
- K203668: RELI NRFit Epidural Needles, Phoenix NRFit Epidural Needles, RELI NRFit Spinal Needles, Phoenix NRFit Spinal Needles (2021), 0 descendants of its own
- K150266: Remington Medical Inc. Tuohy Epidural Needles (2015), 0 descendants of its own

## Indications for use
Spinal and Epidural needles are to be used to inject local anesthetics into a patient to provide regional anesthesia.

Source page: https://510kreport.com/device/K990519
Methodology: https://510kreport.com/methodology