FDA PMA FDA Class 3 Approved 🇺🇸 United States

Agent, Bulking, Injectable For Gastro-Urology Use

PMA: P100014 · Supplement: S004 · Decision Oct 27, 2011
Classifications
1
FEI Numbers
16
Registration Numbers
16

Basic Information

Device Name
Agent, Bulking, Injectable For Gastro-Urology Use
Trade Name
SOLESTA
PMA Number
P100014
Supplement Number
S004
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
October 27, 2011
Date Received
October 13, 2011
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Postapproval Study Protocol - OSB
Expedited Review
N

Advisory Committee Statement

APPROVAL OF THE POST-APPROVAL PROTOCOL.

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