This post-approval study has not been publically released by the fda. It may be a place-holder supplement number.
Device | P170006S013 |
Classification Name | None |
Applicant | |
PMA | P170006 |
Supplement | S013 |
Supplement Number | Date | Supplement Type |
---|---|---|
P170006 | Original Filing | |
S021 | 2022-07-20 | 30-day Notice |
S020 | 2022-02-28 | 30-day Notice |
S019 | 2020-11-25 | 30-day Notice |
S018 | 2020-10-02 | Real-time Process |
S017 | 2020-08-03 | 30-day Notice |
S016 | 2019-09-26 | Real-time Process |
S015 | 2019-06-20 | 30-day Notice |
S014 | 2019-05-31 | 30-day Notice |
S013 | ||
S012 | 2019-05-03 | 30-day Notice |
S011 | 2019-04-18 | 30-day Notice |
S010 | 2019-01-29 | 30-day Notice |
S009 | 2019-01-24 | 30-day Notice |
S008 | 2018-11-21 | 30-day Notice |
S007 | ||
S006 | 2018-07-27 | 30-day Notice |
S005 | 2017-11-22 | 30-day Notice |
S004 | 2017-10-23 | 30-day Notice |
S003 | 2017-10-18 | 30-day Notice |
S002 | ||
S001 | 2017-09-11 | 30-day Notice |
Device ID | PMA | Supp |
---|---|---|
00643169983212 | P170006 | 000 |
00643169983205 | P170006 | 000 |
00643169983199 | P170006 | 000 |
00643169983182 | P170006 | 000 |
00643169983175 | P170006 | 000 |
00643169983229 | P170006 | 024 |
00763000647032 | P170006 | 025 |
00763000647049 | P170006 | 025 |
00763000647056 | P170006 | 025 |
00763000647063 | P170006 | 025 |
00763000647070 | P170006 | 025 |
00763000647025 | P170006 | 025 |