Atlas FDA

BRACAnalysis CDx

FDA premarket approval P140020/S016 · decided 2018-10-16

Approval details

PMA number
P140020
Supplement
S016
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
BRACAnalysis CDx
Generic name
Cancer-related germline gene mutation detection system
Applicant
Myriad Genetic Laboratories
Date received
2018-06-29
Decision date
2018-10-16
Days to decision
109 days
Decision code
APPR
Product code
PJG
Advisory committee
Pathology
Expedited review
No
Location
Salt Lake Cit, UT
Statement
Approval for extending the label claim of the BRACAnalysis CDx® to include treatment and maintenance indications for Rubraca® (rucaparib) in ovarian cancer patients.

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