Last synced on 25 November 2022 at 11:04 pm

INVISALIGN SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081960
510(k) Type
Traditional
Applicant
ALIGN TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2008
Days to Decision
161 days
Submission Type
Summary

INVISALIGN SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081960
510(k) Type
Traditional
Applicant
ALIGN TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2008
Days to Decision
161 days
Submission Type
Summary