Clearance Summary
RETROX TITANIUM TUBE SYSTEM FOR THE RETROX TRANSCUTANEOUS AIR CONDUCTION HEARING AID SYSTEM received FDA 510(k) clearance under submission number K040996, sponsored by Gyrus Ent LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2004-08-20.
- Submission: K040996
- Applicant / Sponsor: Gyrus Ent LLC
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.3950
- Decision date: 2004-08-20
Classification & Regulation
This clearance is catalogued under FDA product code NIX and 21 CFR 874.3950, within the Ear, Nose, Throat review panel as a Class II device.