Ruthless Spine RJB— 510(k) K252615

Name: FDA 510(k) clearance K252615
Creator: U.S. Food and Drug Administration
Published: 2025-09-17

Substantially Equivalent

Ruthless, LLC Dba Ruthless Spine

FDA 510(k) clearance K252615 for Ruthless Spine RJB, Substantially Equivalent on 2025-09-17. Applicant: Ruthless, LLC Dba Ruthless Spine. Device class: 2.

Clearance details

Applicant: Ruthless, LLC Dba Ruthless Spine
Product code: Code QWL
Device class: Class 2
Regulation: 21 CFR 888.4560
Advisory panel: Orthopedic
Date received: 2025-08-19
Decision date: 2025-09-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Irwindale, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code QWL

view all

K243375 — Ruthless Spine RJB2024-11-29
DEN230012 — Ruthless Spine RJB2023-07-14

Data sourced from openFDA. This site is unofficial and independent of the FDA.