FDA PMA FDA Class 3 Approved 🇺🇸 United States

Agent, Bulking, Injectable For Gastro-Urology Use

PMA: P100014 · Supplement: S026 · Decision Oct 9, 2020
Classifications
1
FEI Numbers
16
Registration Numbers
16

Basic Information

Device Name
Agent, Bulking, Injectable For Gastro-Urology Use
Trade Name
Solesta Injectable Gel
PMA Number
P100014
Supplement Number
S026
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 9, 2020
Date Received
April 17, 2020
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Labeling Change - PAS
Expedited Review
N

Advisory Committee Statement

Approval of labeling changes after the final report for the post-approval study (PAS) 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