1Han JK, Marple BF, Smith TL, et al. Int Forum Allergy Rhinol. 2012; 2:271-279.
2Kennedy DW, Wright ED, Goldberg AN. Laryngoscope. 2000; 110(S94):29-31.
3Kennedy DW. Expert Review of Respiratory Medicine. 2012; 6(5):493-498.
The PROPEL sinus implants are intended for use after sinus surgery to maintain patency and to locally deliver steroid to the sinus mucosa: PROPEL for use in the ethmoid sinus, PROPEL Mini for use in the ethmoid sinus and frontal sinus opening, and PROPEL Contour for use in the frontal and maxillary sinus ostia. The implants are intended for use in patients ≥18 years of age. Contraindications include patients with intolerance to mometasone furoate (MF) or a hypersensitivity to bioabsorbable polymers. Safety and effectiveness of the implants in pregnant or nursing females have not been studied. Risks may include, but are not limited to, pain/pressure, displacement of implant, possible side effects of intranasal MF, sinusitis, epistaxis, and infection. For complete prescribing information see IFU at www.IntersectENT.com. Rx only.
The PROPEL® implant, delivery system, and/or the use of the PROPEL® implant/delivery system in a method may be covered by one or more U.S. and/or foreign patents, including U.S. Patent Nos. 7,544,192, 7,662,141, 7,662,142, 7,713,255, 7,951,130, 7,951,131, 7,951,133, 8,109,918, 8,535,707, 8,585,730, 8,585,731, and 8,763,222. Other patent applications are pending. This page is intended to serve as notice under 35 U.S.C. § 287(a). Other patent applications are pending. This page is intended to serve as notice under 35 U.S.C. § 287(a).