Last synced on 14 November 2025 at 11:06 pm

AlphaVent Knotless SP PEEK Anchor

Page Type
Cleared 510(K)
510(k) Number
K233893
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2024
Days to Decision
48 days
Submission Type
Summary

AlphaVent Knotless SP PEEK Anchor

Page Type
Cleared 510(K)
510(k) Number
K233893
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2024
Days to Decision
48 days
Submission Type
Summary