Atlas FDA

Intera 3000 Hepatic Artery Infusion Pump

FDA premarket approval P890055/S084 · decided 2024-03-01

Approval details

PMA number
P890055
Supplement
S084
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Intera 3000 Hepatic Artery Infusion Pump
Generic name
Pump, infusion, implanted, programmable
Applicant
Intera Oncology
Date received
2024-02-01
Decision date
2024-03-01
Days to decision
29 days
Decision code
OK30
Product code
LKK
Advisory committee
General Hospital
Expedited review
No
Location
Newton, MA
Statement
approval for a change in the manufacturing for the capillary tube crimping 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.