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CERAVITAL MIDDLE EAR IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913619
510(k) Type
Traditional
Applicant
FRIEDRICHSFELD MEDIZINTECHNIK AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/1991
Days to Decision
63 days
Submission Type
Statement

CERAVITAL MIDDLE EAR IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913619
510(k) Type
Traditional
Applicant
FRIEDRICHSFELD MEDIZINTECHNIK AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/1991
Days to Decision
63 days
Submission Type
Statement