HYDROXYLAPATITE ALVEOLAR RIDGE MAIN— 510(k) K810382

Name: FDA 510(k) clearance K810382
Creator: U.S. Food and Drug Administration
Published: 1981-03-20

Substantially Equivalent

Carbomedics, Inc.

FDA 510(k) clearance K810382 for HYDROXYLAPATITE ALVEOLAR RIDGE MAIN, Substantially Equivalent on 1981-03-20. Applicant: Carbomedics, Inc.. Device class: 2.

Clearance details

Applicant: Carbomedics, Inc.
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 1981-02-13
Decision date: 1981-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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