Atlas FDA

Propel, Propel Mini and Propel Contour Sinus Implants

FDA premarket approval P100044/S042 · decided 2019-06-27

Approval details

PMA number
P100044
Supplement
S042
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Propel, Propel Mini and Propel Contour Sinus Implants
Generic name
Drug-eluting sinus stent
Applicant
Intersect Ent.
Date received
2019-05-31
Decision date
2019-06-27
Days to decision
27 days
Decision code
OK30
Product code
OWO
Advisory committee
Ear, Nose, Throat
Expedited review
No
Location
Menlo Park, CA
Statement
Modification of incoming quality assurance inspection criteria and titles for the packaging tray and lid components.

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