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PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair Patch

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142447
510(k) Type
Traditional
Applicant
Synovis Life Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2015
Days to Decision
127 days
Submission Type
Summary

PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair Patch

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142447
510(k) Type
Traditional
Applicant
Synovis Life Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2015
Days to Decision
127 days
Submission Type
Summary