Last synced on 18 April 2025 at 11:05 pm

Stryker ProCinch Adjustable Loop Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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