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Stryker ProCinch Adjustable Loop Device

Page Type
Cleared 510(K)
510(k) Number
K210078
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2021
Days to Decision
58 days
Submission Type
Summary

Stryker ProCinch Adjustable Loop Device

Page Type
Cleared 510(K)
510(k) Number
K210078
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2021
Days to Decision
58 days
Submission Type
Summary