Atlas FDA

Codman OR Prep Kits

FDA premarket approval P890055/S076 · decided 2020-12-16

Approval details

PMA number
P890055
Supplement
S076
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Codman OR Prep Kits
Generic name
Pump, infusion, implanted, programmable
Applicant
Intera Oncology
Date received
2020-11-17
Decision date
2020-12-16
Days to decision
29 days
Decision code
OK30
Product code
LKK
Advisory committee
General Hospital
Expedited review
No
Location
Newton, MA
Statement
Replacing one inch refill needles with previously approved 1.5 inch refill needles in OR prep kit and corresponding labeling edits.

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