Last synced on 20 December 2024 at 11:05 pm

Peri-Guard and Supple Peri-Guard

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223052
510(k) Type
Traditional
Applicant
Synovis Life Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2023
Days to Decision
190 days
Submission Type
Summary

Peri-Guard and Supple Peri-Guard

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223052
510(k) Type
Traditional
Applicant
Synovis Life Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2023
Days to Decision
190 days
Submission Type
Summary