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DURAFIBER Ag

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161289
510(k) Type
Traditional
Applicant
SMITH & NEPHEW MEDICAL LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/3/2016
Days to Decision
86 days
Submission Type
Summary

DURAFIBER Ag

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161289
510(k) Type
Traditional
Applicant
SMITH & NEPHEW MEDICAL LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/3/2016
Days to Decision
86 days
Submission Type
Summary