FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Stimulator, Bone Growth, Non-Invasive

PMA: P910066 · Supplement: S029 · Decision Jun 19, 2018
Classifications
1
FEI Numbers
17
Registration Numbers
17

Basic Information

Device Name
Stimulator, Bone Growth, Non-Invasive
Trade Name
OL1000/OL1000 SC and SpinaLogic Bone Growth Stimulators
PMA Number
P910066
Supplement Number
S029
Device Class
FDA Class 3
Product Code
LOF
Generic Name
Stimulator, bone growth, non-invasive
Medical Specialty
Unknown
Advisory Committee
Orthopedic
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
June 19, 2018
Date Received
May 23, 2018
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Change in supplier of the sensor board.

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