Caduceus S— 510(k) K242271

Name: FDA 510(k) clearance K242271
Creator: U.S. Food and Drug Administration
Published: 2024-10-30

Substantially Equivalent

Taiwan Main Orthopaedic Biotechnology Co., Ltd.

FDA 510(k) clearance K242271 for Caduceus S, Substantially Equivalent on 2024-10-30. Applicant: Taiwan Main Orthopaedic Biotechnology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Taiwan Main Orthopaedic Biotechnology Co., Ltd.
Product code: Code SBF
Device class: Class 2
Regulation: 21 CFR 882.4560
Advisory panel: Neurology
Date received: 2024-08-01
Decision date: 2024-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taichung City, TW

Download summary PDF View on FDA.gov ↗

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