Atlas FDA

Codman 3000 Implantable Infusion Pump

FDA premarket approval P890055/S071 · decided 2018-01-12

Approval details

PMA number
P890055
Supplement
S071
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Codman 3000 Implantable Infusion Pump
Generic name
Pump, infusion, implanted, programmable
Applicant
Intera Oncology
Date received
2017-12-13
Decision date
2018-01-12
Days to decision
30 days
Decision code
OK30
Product code
LKK
Advisory committee
General Hospital
Expedited review
No
Location
Newton, MA
Statement
Removal of the streaming potential test for the capillary tubing for the Codman 3000 Constant Flow pump.

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