JAZZ System, including JAZZ Band— 510(k) K170730

Name: FDA 510(k) clearance K170730
Creator: U.S. Food and Drug Administration
Published: 2017-06-09

Substantially Equivalent

Implanet, S.A.

FDA 510(k) clearance K170730 for JAZZ System, including JAZZ Band, Substantially Equivalent on 2017-06-09. Applicant: Implanet, S.A.. Device class: 2.

Clearance details

Applicant: Implanet, S.A.
Product code: Code OWI
Device class: Class 2
Regulation: 21 CFR 888.3010
Advisory panel: Orthopedic
Date received: 2017-03-09
Decision date: 2017-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Martillac, 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.