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BIA300 SERIES IMPLANT AND ABUTMENT, BI300 IMPLANT, BA300 ABUTMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100360
510(k) Type
Traditional
Applicant
COCHLEAR AMERICAS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2010
Days to Decision
151 days
Submission Type
Statement

BIA300 SERIES IMPLANT AND ABUTMENT, BI300 IMPLANT, BA300 ABUTMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100360
510(k) Type
Traditional
Applicant
COCHLEAR AMERICAS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2010
Days to Decision
151 days
Submission Type
Statement