Last synced on 28 June 2024 at 11:05 pm

Spark Clear Aligner System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203737
510(k) Type
Traditional
Applicant
Ormco Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2021
Days to Decision
90 days
Submission Type
Summary

Spark Clear Aligner System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203737
510(k) Type
Traditional
Applicant
Ormco Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2021
Days to Decision
90 days
Submission Type
Summary