RELIEVA SCOUT® Multi-Sinus Dilation System

RELIEVA SCOUT® Multi-Sinus Dilation System

The RELIEVA SCOUT® Multi-Sinus Dilation System includes an Angle Selection Tool that enables predictible bending of the seeker-like tip.

 

Key features:

 

  • Low-profile, seeker-like tip to access tight anatomy and palpate tissue
  • An extendable, illuminated ball tip for atraumatic sinus access and pinpoint, transcutaneous confirmation
  • 6x24mm balloon to dilate ostium and outflow tracks

 

View IFU: Instructions for Use

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Additional Information

  • Catalog Number
    • SCT0624MFS
  • Product
    • RELIEVA SCOUT® Multi-Sinus Dilation System

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ACCLARENT RELIEVA® Balloon Sinuplasty Devices are intended for use by or under the direction of a physician who is trained in the use of Acclarent Technology. ACCLARENT® Balloon Sinuplasty Device use has described risks, including tissue and mucosal trauma, infection, or possible orbital injury.  Prior to use, it is important to read the Instructions for Use and to understand the contraindications, warnings, and precautions associated with these devices, as well as all products mentioned on this resource.  

RELIEVA SPINPLUS® Balloon Sinuplasty System and RELIEVA ULTIRRA® Sinus Balloon Catheter are indicated for dilation of maxillary sinuses in children 17 and younger. All referenced studies below included limited use of the devices in frontal and sphenoid sinuses, for which the safety and effectiveness for children 17 and under has not been establised.

Acclarent Devices are intended for use by or under the direction of a physician who is trained in the use of Acclarent Technology. INSPIRA AIR® Balloon Dilation System use has described risks, including serious complications such as airway obstruction, airway rupture (partial or complete) resulting in pneumomediastinum, pneumothorax and mediastinitis, chest pain, bronchospasm, atelectasis, pulmonary edema and bleeding. Prior to use, it is important to read the Instructions for Use and to understand the contraindications, warnings, and precautions associated with these devices.

The RELIEVA CIRCA® Ethmoid Punch is an instrument for the excision of bone and soft tissue in the ethmoid sinus in adults, and is intended for use by or under the direction of a physician with experience in sinus surgery. The RELIEVA CIRCA® Ethmoid Punch use has described risks including unintended tissue trauma, bleeding and infection. Prior to use, it is important to read the Instructions for Use and to understand the contraindications, warnings and precautions described for this device.

ACCLARENT® ENT Navigation Technology is intended for use by or under the direction of a physician. Devices guided by the Acclarent Navigation Technology have described risks including the potential for unintended injury to the orbits or CNS as a consequence of inaccurate navigation. Prior to use, it is important to read the Instructions for Use and to understand the registration process and the contraindications, warnings and precautions described for the system.

Important information: Prior to use, refer to the instructions for use supplied with this device for indications, contraindications, side effects, warnings and precautions.

Caution: US law restricts this device to sale by or on the order of a physician.

This site is published by Acclarent, Inc. which is soley responsible for its contents. It is intended for visitors from the United States.

© Acclarent, Inc. 2019. Last Updated on November 15, 2018.

1Dearking AC, Pallanch JF. (2012). Mapping the Frontal Sinus Ostia Using Virtual Endoscopy.  Laryngoscope. 122(10):2143-2147.
2Sikand, Ashley. (2011). Computed Tomography-Based Exploration of Infundibular Anatomy for Maxillary Sinus Balloon Dilation.  Annals of Otology, Rhinology & Laryngology. 120(10):656–662.
3Levine HL, Sertich AP, Hoisington DR, et al. (2008). Multicenter Registry of Balloon Catheter Sinusotomy Outcomes for 1,036 Patients.  Annals of Otology, Rhinology & Laryngology. 11(4):263-270.
4Karanfilov B, Silvers S, Pasha R, et al. (2012). ORI0S2 Study Investigators. Office-based Balloon Sinus Dilation: A Prospective, Multicenter Study of 203 Patients.  Int Forum Allergy Rhinology. 3(5):404-411.
5Weiss R, Church CA, Kuhn FA, et al. (2008). Long-Term Outcome Analysis of Balloon Catheter Sinusotomy: Two-Year Follow-Up. Otolaryngolgy-Head and Neck Surgery. 139(3_suppl_1):S38-S46.

 

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