FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AnastoClip GC Closure System

K Number: K173323 · Decision Mar 8, 2018
Classifications
1
FEI Numbers
112
Registration Numbers
112
Same Product Code
175
Applicant Total
32
Review Days
139

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
AnastoClip GC Closure System
K Number
K173323
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
LeMaitre Vascular, Inc.
Date Received
October 20, 2017
Decision Date
March 8, 2018
Product Code
FZP
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FZP Clip, Implantable

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FZP), ordered by most recent decision date.

View all

Other Clearances by LeMaitre Vascular, Inc.

K Number Device Name
K212894 PhasTIPP
K183513 XenoSure Dura Biologic Patch
K152833 Pruitt F3-S Polyurethane Carotid Shunt
K143454 Pruitt F3-S Carotid Shunt
K142660 Antegrade LeMills Valvulotome
K140042 1.5MM HYDRO EXPANDABLE LEMAITRE VALVULOTOME
K133026 UNBALLOON NON-OCCLUSION MODELING CATHETER
K132022 LEMAITRE 8F OCCLUSION CATHETER
K132047 LEMILLS VALVULOTOME
K132190 EXPANDABLE LEMAITRE VALVULOTOME, OVER-THE-WIRE LEMAITRE VALVULOTOME
Search all 32 clearances from LeMaitre Vascular, Inc. →