TRELLIS COLLAGEN RIBBON— 510(k) K131143

Name: FDA 510(k) clearance K131143
Creator: U.S. Food and Drug Administration
Published: 2013-10-07

Substantially Equivalent

Wrightmedicaltechnologyinc

FDA 510(k) clearance K131143 for TRELLIS COLLAGEN RIBBON, Substantially Equivalent on 2013-10-07. Applicant: Wrightmedicaltechnologyinc. Device class: 2.

Clearance details

Applicant: Wrightmedicaltechnologyinc
Product code: Code OWY
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2013-04-23
Decision date: 2013-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, TN, US

Download summary PDF View on FDA.gov ↗

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