Last synced on 30 September 2022 at 11:05 pm

ATOZ Mini-Screw

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210559
510(k) Type
Traditional
Applicant
MK Meditech Inc.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
12/19/2021
Days to Decision
297 days
Submission Type
Summary

ATOZ Mini-Screw

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210559
510(k) Type
Traditional
Applicant
MK Meditech Inc.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
12/19/2021
Days to Decision
297 days
Submission Type
Summary