INTERPORE 200 POROUS HYDROXYAPATITE— 510(k) K860983

Name: FDA 510(k) clearance K860983
Creator: U.S. Food and Drug Administration
Published: 1986-05-23

Substantially Equivalent

Interpore Intl.

FDA 510(k) clearance K860983 for INTERPORE 200 POROUS HYDROXYAPATITE, Substantially Equivalent on 1986-05-23. Applicant: Interpore Intl.. Device class: 2.

Clearance details

Applicant: Interpore Intl.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 1986-03-17
Decision date: 1986-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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