MIMIX MP BONE VOID FILLER— 510(k) K043280

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K043280 for MIMIX MP BONE VOID FILLER, Substantially Equivalent on 2004-12-21. Applicant: Biomet, Inc..

Clearance details

Applicant: Biomet, Inc.
Product code: Code GXP
Advisory panel: Neurology
Date received: 2004-11-26
Decision date: 2004-12-21
Decision: Substantially Equivalent
Clearance type: Special
Location: Warsaw, IN, US

Download summary PDF View on FDA.gov ↗

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