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Bia300 Series Implant And Abutment, Bi300 Implant, Ba300 Abutment
FDA 510(k)Class II (US FDA 510(k))
510(k) K100360
Identifiers
- 510(k) Number
- K100360 FDA 510(k)
- FDA Product Code
- LXB FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 874.3302 FDA 510(k)
- Regulation Number
- 874.3302 FDA 510(k)
- Advisory Committee
- Ear, Nose, Throat FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Bia300 Series Implant And Abutment, Bi300 Implant, Ba300 Abutment by Cochlear Americas — Class II — FDA_510K — listed in FDA 510(k)
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K100360 | Class II | Active |
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Manufacturer
- Manufacturer
- Cochlear Americas
Sources (1)
- FDA 510(k) K100360 24 fields · synced Jun 18, 2026