FDA PMA FDA Class 3 Approved 🇺🇸 United States

Stimulator, Bone Growth, Non-Invasive

PMA: P030034 · Supplement: S004 · Decision Jan 12, 2011
Classifications
1
FEI Numbers
17
Registration Numbers
17

Basic Information

Device Name
Stimulator, Bone Growth, Non-Invasive
Trade Name
CERVICAL-STIM
PMA Number
P030034
Supplement Number
S004
Device Class
FDA Class 3
Product Code
LOF
Generic Name
Stimulator, bone growth, non-invasive
Medical Specialty
Unknown
Advisory Committee
Orthopedic
Decision
Approved
Decision Code
APPR
Decision Date
January 12, 2011
Date Received
January 21, 2010
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 LOCATED IN LEWISVILLE, TEXAS.

Classifications

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

Product Code Device Name
LOF Stimulator, Bone Growth, Non-Invasive