KLS-MARTIN TEMPORARY CONDYLAR IMPLANT— 510(k) K990667

Name: FDA 510(k) clearance K990667
Creator: U.S. Food and Drug Administration
Published: 2001-07-27

Substantially Equivalent

KLS-Martin L.P.

FDA 510(k) clearance K990667 for KLS-MARTIN TEMPORARY CONDYLAR IMPLANT, Substantially Equivalent on 2001-07-27. Applicant: KLS-Martin L.P.. Device class: 2.

Clearance details

Applicant: KLS-Martin L.P.
Product code: Code NEI
Device class: Class 2
Regulation: 21 CFR 872.4770
Advisory panel: Dental
Date received: 1999-03-02
Decision date: 2001-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Port Riche, FL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.