Nunchaku— 510(k) K161373

Name: FDA 510(k) clearance K161373
Creator: U.S. Food and Drug Administration
Published: 2016-11-03

Substantially Equivalent

Fci (France Chirurgie Instrumentation)

FDA 510(k) clearance K161373 for Nunchaku, Substantially Equivalent on 2016-11-03. Applicant: Fci (France Chirurgie Instrumentation). Device class: Unclassified.

Clearance details

Applicant: Fci (France Chirurgie Instrumentation)
Product code: Code OKS
Device class: Unclassified
Advisory panel: Unknown
Date received: 2016-05-17
Decision date: 2016-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paris, FR

Download summary PDF View on FDA.gov ↗

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