POREX(TM) PROSTHESIS, CHIN, INTERNAL— 510(k) K863941

Name: FDA 510(k) clearance K863941
Creator: U.S. Food and Drug Administration
Published: 1986-10-24

Substantially Equivalent

Porex Medical

FDA 510(k) clearance K863941 for POREX(TM) PROSTHESIS, CHIN, INTERNAL, Substantially Equivalent on 1986-10-24. Applicant: Porex Medical. Device class: 2.

Clearance details

Applicant: Porex Medical
Product code: Code FWP
Device class: Class 2
Regulation: 21 CFR 878.3550
Advisory panel: General, Plastic Surgery
Date received: 1986-10-10
Decision date: 1986-10-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fairburn, GA, 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.