PIEZOSURGERY DEVICE— 510(k) K043408

Substantially Equivalent

Piezosurgery S.R.L.

FDA 510(k) clearance K043408 for PIEZOSURGERY DEVICE, Substantially Equivalent on 2005-06-08. Applicant: Piezosurgery S.R.L.. Device class: 2.

Clearance details

Applicant: Piezosurgery S.R.L.
Product code: Code DZI
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2004-12-10
Decision date: 2005-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rome, IT

Download summary PDF View on FDA.gov ↗

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More clearances from Piezosurgery S.R.L.

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