Atlas FDA

COLOGUARD

FDA premarket approval P130017/S026 · decided 2019-03-11

Approval details

PMA number
P130017
Supplement
S026
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
COLOGUARD
Generic name
System, colorectal neoplasia, DNA methylation and hemoglobin detection
Applicant
Exact Sciences Corporation
Date received
2019-02-07
Decision date
2019-03-11
Days to decision
32 days
Decision code
OK30
Product code
PHP
Advisory committee
Pathology
Expedited review
No
Location
Medison, WI
Statement
Scale-up of components in the Cologuard sDNA based colorectal cancer screening test.

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