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BAHA CORDELLE II

Page Type
Cleared 510(K)
510(k) Number
K080363
510(k) Type
Traditional
Applicant
COCHLEAR BONE ANCHORED SYSTEMS AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2008
Days to Decision
59 days
Submission Type
Summary

BAHA CORDELLE II

Page Type
Cleared 510(K)
510(k) Number
K080363
510(k) Type
Traditional
Applicant
COCHLEAR BONE ANCHORED SYSTEMS AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2008
Days to Decision
59 days
Submission Type
Summary