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FDA 510(k)

Ruthless Spine RJB

K-Number: K252615 · 2025-09-17

Decision Date2025-09-17
Product CodeQWL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Ruthless Spine RJB is the device name listed in this FDA 510(k) record. The listed applicant is Ruthless, LLC Dba Ruthless Spine. It received FDA 510(k) clearance on 2025-09-17 under 510(k) number K252615. 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 2025-09-17. The listed applicant is Ruthless, LLC Dba Ruthless Spine. The 510(k) number is K252615.

When did Ruthless Spine RJB receive FDA 510(k) clearance?

Ruthless Spine RJB received FDA 510(k) clearance on 2025-09-17, under 510(k) number K252615.

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

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