Atlas FDA

BRACAnalysis CDx

FDA premarket approval P140020/S018 · decided 2018-12-19

Approval details

PMA number
P140020
Supplement
S018
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
2018-09-21
Decision date
2018-12-19
Days to decision
89 days
Decision code
APPR
Product code
PJG
Advisory committee
Pathology
Expedited review
No
Location
Salt Lake Cit, UT
Statement
Approval for the BRACAnalysis CDx®, for gBRCA mutated ovarian cancer patients maintenance monotherapy with Lynparza® (olaparib).

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