MODIFICATION TO: INJECTABLE MIMIX— 510(k) K012569

Substantially Equivalent

Biomet, Inc.

FDA 510(k) clearance K012569 for MODIFICATION TO: INJECTABLE MIMIX, Substantially Equivalent on 2001-12-21. Applicant: Biomet, Inc.. Device class: 2.

Clearance details

Applicant: Biomet, Inc.
Product code: Code GXP
Device class: Class 2
Regulation: 21 CFR 882.5300
Advisory panel: Neurology
Date received: 2001-08-09
Decision date: 2001-12-21
Decision: Substantially Equivalent
Clearance type: Special
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.