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Spinal Frontiers · Regulatory Watch · FDA decision

Spinal Simplicity clears updated interspinous plates and SI implants

FDA decision · Spinal Simplicity

2 October 2026

A single 510(k) covered several Minuteman spinous-process fusion plates and the company's Patriot and Liberty lateral sacroiliac joint implants.

Type: FDA decision
Company: Spinal Simplicity
Device: Minuteman MIS fusion plates; Patriot SI and Liberty SI Lateral implant systems
Date: 2 October 2026
Jurisdiction: US
Classification: 510(k) K261607 (PEK; OUR)
Source: FDA 510(k) database

Official source →Source checked

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