PMA P850022S034

Device
Biomet® SpinalPak® Non-invasive Spine Fusion Stimulator System, Biomet® OrthoPak® Non-invasive Bone Growth Stimulator Sy
Applicant
Ahp Eos Buyer, Inc.
PMA number
P850022
Supplement
S034
Product code
LOF
Decision date
2024-02-29
Classification
Orthopedic
Generic name
Stimulator, bone growth, non-invasive
Approval order statement
Approval for a minor material change to the patient lead cable insulation (i.e., the extruded jacket).

Current openFDA PMA Record#

Device
Biomet® SpinalPak® Non-invasive Spine Fusion Stimulator System, Biomet® OrthoPak® Non-invasive Bone Growth Stimulator Sy
Applicant
Ahp Eos Buyer, Inc.
PMA number
P850022
Supplement
S034
Product code
LOF
Generic name
Stimulator, bone growth, non-invasive
Decision date
2024-02-29
Decision code
APPR
Date received
2023-12-01
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Approval order statement
Approval for a minor material change to the patient lead cable insulation (i.e., the extruded jacket).