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LARYNGEAL AUGMENTATION IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K033398
510(k) Type
Traditional
Applicant
BIOFORM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/2003
Days to Decision
49 days
Submission Type
Summary

LARYNGEAL AUGMENTATION IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K033398
510(k) Type
Traditional
Applicant
BIOFORM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/2003
Days to Decision
49 days
Submission Type
Summary