This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.
Approval for the cobas® 4800 braf v600 mutation test. The cobas® 4800 braf v600 mutation test is an in vitro diagnostic device intended for the qualitative detection of braf v600e mutation in dna extracted from formalin-fixed, paraffin-embedded human melanoma tissue. The cobas® 4800 braf v600 mutation test is a real-time pcr test on the cobas® 4800 system, and is intended to be used as an aid in selecting melanoma patients for treatment with the targeted therapies listed in the table below, in accordance with the approved therapeutic product labeling: therapeutic therapeutic indication test resultzelboraf® (vemurafenib) braf v600e mutation detectedcotellic® (cobimetinib), in combination with zelboraf® (vemurafenib) braf v600e or v600k* mutation detected* *due to cross-reactivity by the cobas® 4800 braf v600 mutation test, the clinical trial for cobimetinib, in combination with vemurafenib, included some patients whose tumor carried the braf v600k mutation.
Device | Roche cobas DNA Sample Preparation Kit, COBAS 4800 BRAF V600 MUTATION TEST |
Classification Name | Somatic Gene Mutation Detection System |
Generic Name | Somatic Gene Mutation Detection System |
Applicant | Roche Molecular Systems, Inc. |
Date Received | 2016-06-30 |
Decision Date | 2016-11-07 |
PMA | P110020 |
Supplement | S016 |
Product Code | OWD |
Advisory Committee | Pathology |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Change Design/components/specifications/material |
Expedited Review | No |
Combination Product | No |
Applicant Address | Roche Molecular Systems, Inc. 4300 Hacienda Drive pleasanton, CA 94588-2722 |
Supplement Number | Date | Supplement Type |
---|---|---|
P110020 | Original Filing | |
S037 | 2022-10-21 | 30-day Notice |
S036 | ||
S035 | 2020-07-27 | 30-day Notice |
S034 | 2019-09-20 | 30-day Notice |
S033 | 2019-06-27 | Real-time Process |
S032 | 2019-04-24 | 30-day Notice |
S031 | 2018-11-13 | 30-day Notice |
S030 | 2018-11-09 | 30-day Notice |
S029 | 2018-08-21 | 30-day Notice |
S028 | 2018-07-27 | 30-day Notice |
S027 | 2018-06-29 | 30-day Notice |
S026 | 2018-06-08 | 30-day Notice |
S025 | 2018-06-04 | 30-day Notice |
S024 | 2018-03-01 | 30-day Notice |
S023 | 2017-10-30 | 30-day Notice |
S022 | 2017-09-26 | 30-day Notice |
S021 | 2017-07-17 | 30-day Notice |
S020 | 2017-07-14 | 30-day Notice |
S019 | 2017-07-14 | 30-day Notice |
S018 | 2016-08-22 | 30-day Notice |
S017 | 2016-07-08 | 30-day Notice |
S016 | 2016-06-30 | Normal 180 Day Track |
S015 | 2016-04-18 | 30-day Notice |
S014 | 2015-06-24 | 30-day Notice |
S013 | 2015-03-13 | 30-day Notice |
S012 | 2014-12-19 | 30-day Notice |
S011 | 2013-12-13 | 30-day Notice |
S010 | 2013-12-13 | Real-time Process |
S009 | 2013-08-14 | 30-day Notice |
S008 | 2013-08-09 | 30-day Notice |
S007 | 2013-07-26 | 30-day Notice |
S006 | 2012-09-12 | Normal 180 Day Track |
S005 | 2012-08-15 | 30-day Notice |
S004 | 2012-07-02 | Real-time Process |
S003 | 2011-12-12 | 135 Review Track For 30-day Notice |
S002 | 2011-09-29 | 30-day Notice |
S001 | 2011-09-19 | 30-day Notice |