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Alpha Vent PEEK Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K211502
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/2021
Days to Decision
82 days
Submission Type
Summary

Alpha Vent PEEK Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K211502
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/2021
Days to Decision
82 days
Submission Type
Summary