XYLOS VESSEL GUARD— 510(k) K100984

Unknown

Xylos Corporation

FDA 510(k) clearance K100984 for XYLOS VESSEL GUARD, Unknown on 2010-07-07. Applicant: Xylos Corporation. Device class: 2.

Clearance details

Applicant: Xylos Corporation
Product code: Code OMR
Device class: Class 2
Regulation: 21 CFR 870.3470
Advisory panel: Cardiovascular
Date received: 2010-04-08
Decision date: 2010-07-07
Decision: Unknown
Clearance type: Traditional
Location: Langhorne, PA, US

Download summary PDF View on FDA.gov ↗

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K083823 — SECURIAN TISSUE REINFORCEMENT MATRIX2009-03-18
K081882 — MODIFICATION TO XYLOS SURGICAL MESH2008-07-11

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