VITOMATRIX— 510(k) K091618

Substantially Equivalent

Orthovita, Inc.

FDA 510(k) clearance K091618 for VITOMATRIX, Substantially Equivalent on 2010-09-27. Applicant: Orthovita, Inc.. Device class: 2.

Clearance details

Applicant: Orthovita, Inc.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2009-06-03
Decision date: 2010-09-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Malver, PA, US

Download summary PDF View on FDA.gov ↗

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