# K203668: RELI NRFit Epidural Needles, Phoenix NRFit Epidural Needles, RELI NRFit Spinal Needles, Phoenix NRFit Spinal Needles

- Pathway: 510(k) (Traditional)
- Applicant: Myco Medical Supplies, Inc.
- Decided: Sep 29, 2021 after 287 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
Longest line of descent: 2 generations back to K990519 (2000). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183316: Dr J Spinal and Epidural Needles, Dr. Japan Co., Ltd. (2019) Summary page 4.

## 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/K203668
Methodology: https://510kreport.com/methodology