Approximately thirty subjects with mixed or conductive hearing loss, meeting FDA-cleared candidacy criteria for the BONEBRIDGE, will be implanted and followed for three (3) months post-activation to assess safety and effectiveness of the BONEBRIDGE implant.
| Condition | Mixed conductive and sensorineural hearing loss, Conductive hearing loss, mixed hearing loss |
|---|---|
| Treatment | Bonebridge |
| Clinical Study Identifier | NCT03859648 |
| Sponsor | Med-El Corporation |
| Last Modified on | 22 April 2021 |
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