Ruthless Spine RJB
K-Number: K243375 · 2024-11-29
ApplicantRuthless, LLC Dba Ruthless Spine
Decision Date2024-11-29
Product CodeQWL
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Ruthless Spine RJB is a medical device manufactured by Ruthless, LLC Dba Ruthless Spine. It received FDA 510(k) clearance on 2024-11-29 under approval number K243375. The device is classified under product code QWL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Ruthless, LLC Dba Ruthless Spine. The 510(k) number is K243375.
When was Ruthless Spine RJB approved by the FDA?
Ruthless Spine RJB received FDA 510(k) clearance on 2024-11-29, under approval number K243375.
What company makes Ruthless Spine RJB?
Ruthless Spine RJB is manufactured by Ruthless, LLC Dba Ruthless Spine.
What is the FDA product code for Ruthless Spine RJB?
The FDA product code for Ruthless Spine RJB is QWL.
Other Devices by Ruthless, LLC Dba Ruthless Spine
Related Devices (Code: QWL)
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.