Atlas FDA

Propel Mini Sinus Implant

FDA premarket approval P100044/S038 · decided 2019-07-24

Approval details

PMA number
P100044
Supplement
S038
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Propel Mini Sinus Implant
Generic name
Drug-eluting sinus stent
Applicant
Intersect Ent.
Date received
2019-04-25
Decision date
2019-07-24
Days to decision
90 days
Decision code
APPR
Product code
OWO
Advisory committee
Ear, Nose, Throat
Expedited review
No
Location
Menlo Park, CA
Statement
Approval for the introduction of a delivery system with a straight applicator for ethmoid sinus access and serves as an alternative to the approved delivery system with a curved applicator.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
VenSure LightGuide (K212774)Intersect Ent.2022-02-04