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Sinus surgery is only part of the battle.

Add PROPEL to your
ACTION PLAN

For adult patients with chronic rhinosinusitis (CRS) following ethmoid, frontal, or maxillary sinus surgery

STRENGTHEN YOUR SINUS SURGERY ARMAMENTARIUM WITH THE PROPEL FAMILY OF IMPLANTS

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Arm yourself to maintain sinus patency and reduce:

  • postoperative interventions
  • frank polyposis
  • occlusion/restenosis
  • inflammation
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MAXILLARY
SINUS

FRONTAL
SINUS

ETHMOID
SINUS

ethmoid sinus

PROPEL

frontal sinus ethmoid sinus

PROPEL MINI

frontal sinus maxillary sinus

PROPEL
CONTOUR

STRENGTHEN YOUR SINUS SURGERY ARMAMENTARIUM WITH THE PROPEL FAMILY OF IMPLANTS

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s
Adding to an arsenal of PROPEL evidence. The first of its kind ENT real-world evidence study.
CMR Publication

THE USE OF PROPEL FOLLOWING SINUS SURGERY MAY RESULT IN PAYER SAVINGS FROM REDUCED HEALTHCARE RESOURCE UTILIZATION.

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Patients with CRS may benefit from postoperative care that reduces inflammation, in order to achieve improved sinus surgery outcomes

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STRENGTHEN YOUR SINUS SURGERY ARMAMENTARIUM WITH THE PROPEL FAMILY OF IMPLANTS

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6 REASONS TO ADD THE PROPEL FAMILY OF IMPLANTS TO YOUR SINUS SURGERY PLAN

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Resources and Downloads

The following resources may be helpful to further educate yourself about PROPEL and how to implement PROPEL into your practice

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This site is intended for healthcare professionals in the United States

Instructions for Use:

PROPEL PROPEL MINI PROPEL MINI WITH SDS PROPEL CONTOUR
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References

  1. PROPEL [Instructions for Use]. Menlo Park, CA: Intersect ENT; 2013.
  2. PROPEL Mini [Instructions for Use]. Menlo Park, CA: Intersect ENT; 2016.
  3. PROPEL Contour [Instructions for Use]. Menlo Park, CA: Intersect ENT; 2016.

The PROPEL sinus implants are intended to maintain patency and locally deliver steroid to the sinus mucosa in patients ≥18 years of age following sinus surgery: PROPEL for the ethmoid sinus, PROPEL Mini for the ethmoid sinus/frontal sinus opening, and PROPEL Contour for the frontal/maxillary sinus ostia. Contraindications include patients with confirmed hypersensitivity or intolerance to mometasone furoate (MF) or hypersensitivity to bioabsorbable polymers. Safety and effectiveness of the implant in pregnant or nursing females have not been studied. Risks may include, but are not limited to, pain/pressure, displacement of the implant, possible side effects of intranasal MF, sinusitis, epistaxis, and infection. For full prescribing information see IFU at www.IntersectENT.com/technologies/. Rx only.

© 2024 Intersect ENT, Inc. All rights reserved. Intersect ENT and PROPEL are registered trademarks of Intersect ENT, Inc. in the United States and other countries. MPM-11549 Rev 7.0

The above-identified implants, delivery systems, and/or the use of the above-identified implants/delivery systems in a method may be covered by one or more U.S. and/foreign patents, found at intersectent.com/patents.