Last synced on 20 December 2024 at 11:05 pm

High Retention Attachment System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213391
510(k) Type
Traditional
Applicant
Zest Anchors, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2022
Days to Decision
88 days
Submission Type
Summary

High Retention Attachment System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213391
510(k) Type
Traditional
Applicant
Zest Anchors, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2022
Days to Decision
88 days
Submission Type
Summary