G-FLOSS & G-FLOSS II— 510(k) K911701

Name: FDA 510(k) clearance K911701
Creator: U.S. Food and Drug Administration
Published: 1991-05-15

Substantially Equivalent

Implant Innovations International, Inc.

FDA 510(k) clearance K911701 for G-FLOSS & G-FLOSS II, Substantially Equivalent on 1991-05-15. Applicant: Implant Innovations International, Inc.. Device class: 1.

Clearance details

Applicant: Implant Innovations International, Inc.
Product code: Code JES
Device class: Class 1
Regulation: 21 CFR 872.6390
Advisory panel: Dental
Date received: 1991-04-16
Decision date: 1991-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Palm Beach, FL, US

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