DIGIMATCH ORTHODOC ROBODOC ENCORE SURGICAL SYSTEM— 510(k) K140038

Name: FDA 510(k) clearance K140038
Creator: U.S. Food and Drug Administration
Published: 2014-05-27

Substantially Equivalent

Curexo Technology Corporation

FDA 510(k) clearance K140038 for DIGIMATCH ORTHODOC ROBODOC ENCORE SURGICAL SYSTEM, Substantially Equivalent on 2014-05-27. Applicant: Curexo Technology Corporation. Device class: 2.

Clearance details

Applicant: Curexo Technology Corporation
Product code: Code OJP
Device class: Class 2
Regulation: 21 CFR 882.4560
Advisory panel: Neurology
Date received: 2014-01-07
Decision date: 2014-05-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melrose, MA, US

Download summary PDF View on FDA.gov ↗

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