Modify the handle tensile strength specification for the delivery system for the propel contour sinus implant.
| Device | Propel Contour Sinus Implant |
| Classification Name | Drug-eluting Sinus Stent |
| Generic Name | Drug-eluting Sinus Stent |
| Applicant | INTERSECT ENT |
| Date Received | 2018-06-08 |
| Decision Date | 2018-06-28 |
| PMA | P100044 |
| Supplement | S033 |
| Product Code | OWO |
| Docket Number | Premarket Approval (PMA) // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices Radia |
| Advisory Committee | Ear Nose & Throat |
| Supplement Type | 30-day Notice |
| Supplement Reason | Process Change - Manufacturer/sterilizer/packager/supplier |
| Expedited Review | No |
| Combination Product | Yes |
| Applicant Address | INTERSECT ENT 1555 Adams Dr menlo Park, CA 94025 |
Supplemental Filings
| Supplement Number | Date | Supplement Type |
|---|
| P100044 | | Original Filing |
| S051 |
2022-11-25 |
30-day Notice |
| S050 |
2022-10-05 |
Special (immediate Track) |
| S049 |
2022-03-28 |
Real-time Process |
| S048 |
2021-01-11 |
Real-time Process |
| S047 | | |
| S046 |
2020-04-02 |
Real-time Process |
| S045 |
2020-03-26 |
Special (immediate Track) |
| S044 |
2019-09-10 |
30-day Notice |
| S043 | | |
| S042 |
2019-05-31 |
30-day Notice |
| S041 |
2019-05-03 |
30-day Notice |
| S040 |
2019-05-01 |
30-day Notice |
| S039 |
2019-04-26 |
30-day Notice |
| S038 | | |
| S037 |
2018-11-30 |
Real-time Process |
| S036 |
2018-10-12 |
Real-time Process |
| S035 |
2018-08-24 |
30-day Notice |
| S034 |
2018-08-08 |
30-day Notice |
| S033 |
2018-06-08 |
30-day Notice |
| S032 |
2018-05-02 |
30-day Notice |
| S031 |
2017-09-08 |
Special (immediate Track) |
| S030 |
2017-08-29 |
30-day Notice |
| S029 |
2017-05-30 |
30-day Notice |
| S028 |
2017-04-27 |
30-day Notice |
| S027 |
2017-03-01 |
Real-time Process |
| S026 |
2016-12-27 |
30-day Notice |
| S025 |
2016-09-30 |
30-day Notice |
| S024 |
2016-09-28 |
30-day Notice |
| S023 |
2016-08-01 |
Panel Track |
| S022 |
2016-06-16 |
135 Review Track For 30-day Notice |
| S021 |
2016-05-18 |
30-day Notice |
| S020 |
2016-03-25 |
Normal 180 Day Track No User Fee |
| S019 |
2015-09-30 |
30-day Notice |
| S018 |
2015-09-25 |
Panel Track |
| S017 |
2015-04-02 |
Normal 180 Day Track No User Fee |
| S016 |
2014-04-23 |
30-day Notice |
| S015 |
2014-01-16 |
30-day Notice |
| S014 |
2013-11-12 |
30-day Notice |
| S013 |
2013-11-04 |
Real-time Process |
| S012 |
2013-09-30 |
Normal 180 Day Track No User Fee |
| S011 |
2013-08-21 |
30-day Notice |
| S010 |
2013-06-25 |
Special (immediate Track) |
| S009 | | |
| S008 |
2013-03-04 |
Normal 180 Day Track No User Fee |
| S007 |
2013-01-29 |
30-day Notice |
| S006 |
2012-12-26 |
Normal 180 Day Track No User Fee |
| S005 |
2012-12-20 |
30-day Notice |
| S004 |
2012-12-14 |
Normal 180 Day Track No User Fee |
| S003 |
2012-10-01 |
Real-time Process |
| S002 |
2012-07-31 |
30-day Notice |
| S001 |
2012-03-12 |
Normal 180 Day Track |
NIH GUDID Devices