FDA PMA FDA Class 3 Approved 🇺🇸 United States

Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-Filled

PMA: P230005 · Supplement: S001 · Decision Nov 22, 2024
Classifications
1
FEI Numbers
9
Registration Numbers
9

Basic Information

Device Name
Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-Filled
Trade Name
Motiva SmoothSilk Round Ergonomix Silicone Gel-Filled Breast Implants, Motiva SmoothSilk Round Silicone Gel-Filled Breas
PMA Number
P230005
Supplement Number
S001
Device Class
FDA Class 3
Product Code
FTR
Generic Name
Prosthesis, breast, noninflatable, internal, silicone gel-filled
Regulation Number
878.3540
Medical Specialty
General, Plastic Surgery
Advisory Committee
General, Plastic Surgery
Decision
Approved
Decision Code
APPR
Decision Date
November 22, 2024
Date Received
October 25, 2024
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Postapproval Study Protocol
Expedited Review
N

Advisory Committee Statement

Approval of the protocol for the post-approval study (PAS)

Classifications

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

Product Code Device Name
FTR Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-Filled