MEDPOR PTERIONAL SURGICAL IMPLANT— 510(k) K002586

Name: FDA 510(k) clearance K002586
Creator: U.S. Food and Drug Administration
Published: 2000-11-17

Substantially Equivalent

Porex Surgical Products Group

FDA 510(k) clearance K002586 for MEDPOR PTERIONAL SURGICAL IMPLANT, Substantially Equivalent on 2000-11-17. Applicant: Porex Surgical Products Group. Device class: 2.

Clearance details

Applicant: Porex Surgical Products Group
Product code: Code MNF
Device class: Class 2
Regulation: 21 CFR 878.3550
Advisory panel: General, Plastic Surgery
Date received: 2000-08-21
Decision date: 2000-11-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newnan, GA, US

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