THE STERN ROOT ANCHOR SYSTEM— 510(k) K950213

Name: FDA 510(k) clearance K950213
Creator: U.S. Food and Drug Administration
Published: 1995-03-23

Substantially Equivalent

Sterngold/Implamed

FDA 510(k) clearance K950213 for THE STERN ROOT ANCHOR SYSTEM, Substantially Equivalent on 1995-03-23. Applicant: Sterngold/Implamed. Device class: 1.

Clearance details

Applicant: Sterngold/Implamed
Product code: Code ELR
Device class: Class 1
Regulation: 21 CFR 872.3810
Advisory panel: Dental
Date received: 1995-01-19
Decision date: 1995-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunrise, FL, US

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