510(k) K043191

Device
REPOL ANGIMESH, ANGIMESH PRE, FOLDED MESH, REPOL PLUG BASIC, REPOL PLUG CAP, REPOL PLUG FLOWER AND WINGS MESH
Applicant
Angiologica B. M. Srl
510(k) number
K043191
Product code
FTL
Decision
Substantially Equivalent (SESE)
Decision date
2005-05-16
Date received
2004-11-17
Regulation
878.3300
Classification name
Mesh, Surgical, Polymeric
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
ROBERTO MANCA
Address
4, Via Giovanni Xxiii San Martino Siccomario, Pavia IT 27028 27028

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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