INTERPORE 200 POROUS HYDROXYAPATITE— 510(k) K852975

Name: FDA 510(k) clearance K852975
Creator: U.S. Food and Drug Administration
Published: 1985-10-31

Substantially Equivalent

Inrterpore Intl.

FDA 510(k) clearance K852975 for INTERPORE 200 POROUS HYDROXYAPATITE, Substantially Equivalent on 1985-10-31. Applicant: Inrterpore Intl.. Device class: 1.

Clearance details

Applicant: Inrterpore Intl.
Product code: Code DZC
Device class: Class 1
Regulation: 21 CFR 872.5410
Advisory panel: Dental
Date received: 1985-07-15
Decision date: 1985-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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