REGENEROSS ALLOGRAFT PLUS MINERLIZED— 510(k) K113645

Name: FDA 510(k) clearance K113645
Creator: U.S. Food and Drug Administration
Published: 2012-01-20

Substantially Equivalent

Biomet Interpore Cross

FDA 510(k) clearance K113645 for REGENEROSS ALLOGRAFT PLUS MINERLIZED, Substantially Equivalent on 2012-01-20. Applicant: Biomet Interpore Cross. Device class: 2.

Clearance details

Applicant: Biomet Interpore Cross
Product code: Code NUN
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2011-12-12
Decision date: 2012-01-20
Decision: Substantially Equivalent
Clearance type: Special
Location: Irvine, CA, 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.