MIMIX BONE REPLACEMENT SYSTEM— 510(k) K003494

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K003494 for MIMIX BONE REPLACEMENT SYSTEM, Substantially Equivalent on 2001-04-09. Applicant: Biomet, Inc.. Device class: 2.

Clearance details

Applicant: Biomet, Inc.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2000-11-13
Decision date: 2001-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, 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.