Last synced on 18 April 2025 at 11:05 pm

Knotilus+ PEEK Knotless Anchor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232683
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2023
Days to Decision
53 days
Submission Type
Summary

Knotilus+ PEEK Knotless Anchor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232683
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2023
Days to Decision
53 days
Submission Type
Summary