Ruthless Spine RJB
K-Number: K243375 · 2024-11-29
Device Summary
Frequently Asked Questions
What is the Ruthless Spine RJB?
Ruthless Spine RJB is a medical device that received FDA 510(k) clearance on 2024-11-29. The listed applicant is Ruthless, LLC Dba Ruthless Spine. The 510(k) number is K243375.
When did Ruthless Spine RJB receive FDA 510(k) clearance?
Ruthless Spine RJB received FDA 510(k) clearance on 2024-11-29, under 510(k) number K243375.
Who is the listed applicant for Ruthless Spine RJB?
The FDA 510(k) record lists Ruthless, LLC Dba Ruthless Spine as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ruthless Spine RJB?
The FDA product code for Ruthless Spine RJB is QWL.
Other records listing Ruthless, LLC Dba Ruthless Spine as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: QWL)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.