Last synced on 2 December 2022 at 11:04 pm

LARYNGEAL AUGMENTATION IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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