PROPEL Contour Sinus Implant Delivery System
FDA premarket approval P100044/S029 · decided 2017-06-28
Approval details
- PMA number
- P100044
- Supplement
- S029
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- PROPEL Contour Sinus Implant Delivery System
- Generic name
- Drug-eluting sinus stent
- Applicant
- Intersect Ent.
- Date received
- 2017-05-30
- Decision date
- 2017-06-28
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- OWO
- Advisory committee
- Ear, Nose, Throat
- Expedited review
- No
- Location
- Menlo Park, CA
- Statement
- Changes to the tip molding and the applicator forming manufacturing processes for the Propel Contour Sinus Implant Delivery System.
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510(k) clearances by this applicant
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