SICAGE System— 510(k) K170475

Name: FDA 510(k) clearance K170475
Creator: U.S. Food and Drug Administration
Published: 2017-05-05

Substantially Equivalent

Sicage, LLC

FDA 510(k) clearance K170475 for SICAGE System, Substantially Equivalent on 2017-05-05. Applicant: Sicage, LLC. Device class: 2.

Clearance details

Applicant: Sicage, LLC
Product code: Code OUR
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 2017-02-16
Decision date: 2017-05-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Souix Falls, SD, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code OUR

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K260477 — CATAMARAN SI Joint Fusion System2026-04-08
K253488 — iFuse INTRA Ti Implant System2026-02-11
K253611 — Falco Fusion System2026-01-29
K252834 — Sacroiliac Joint Truss System (SJTS)2026-01-28

Adverse events under product code OUR

product code OUR

Death: 3
Injury: 347
Total: 350

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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