Atlas FDA

ALGOVITA SPINAL CORD STIMULATION SYSTEM

FDA premarket approval P130028/S007 · decided 2016-06-08

Approval details

PMA number
P130028
Supplement
S007
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
ALGOVITA SPINAL CORD STIMULATION SYSTEM
Generic name
Stimulator, spinal-cord, totally implanted for pain relief
Applicant
Nuvectra Corporation
Date received
2016-04-29
Decision date
2016-06-08
Days to decision
40 days
Decision code
OK30
Product code
LGW
Advisory committee
Neurology
Expedited review
No
Location
Blaine, MN
Statement
Changes to the workflow for the Clinician Programmer Printed Circuit Board manufacturing process.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.