BIA300 SERIES IMPLANT AND ABUTMENT, BI300 IMPLANT, BA300 ABUTMENT— 510(k) K100360

Substantially Equivalent

Cochlear Americas

FDA 510(k) clearance K100360 for BIA300 SERIES IMPLANT AND ABUTMENT, BI300 IMPLANT, BA300 ABUTMENT, Substantially Equivalent on 2010-07-13. Applicant: Cochlear Americas. Device class: 2.

Clearance details

Applicant
Cochlear Americas
Product code
Code LXB
Device class
Class 2
Regulation
21 CFR 874.3302
Advisory panel
Ear, Nose, Throat
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Centennial, CO, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code LXB

product code LXB
Injury
2,334
Total
2,334

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.