FDA PMA FDA Class 3 Approved 🇺🇸 United States

Agent, Bulking, Injectable For Gastro-Urology Use

PMA: P040050 · Supplement: S001 · Decision Jul 27, 2007
Classifications
1
FEI Numbers
16
Registration Numbers
16

Basic Information

Device Name
Agent, Bulking, Injectable For Gastro-Urology Use
Trade Name
MACROPLASTIQUE IMPLANTS
PMA Number
P040050
Supplement Number
S001
Device Class
FDA Class 3
Product Code
LNM
Generic Name
AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
Medical Specialty
Unknown
Advisory Committee
Gastroenterology, Urology
Decision
Approved
Decision Code
APPR
Decision Date
July 27, 2007
Date Received
March 2, 2007
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A MANUFACTURING SITE CHANGE FROM MINNEAPOLIS, MINNESOTA TO MINNETONKA, MINNESOTA.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LNM Agent, Bulking, Injectable For Gastro-Urology Use