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Smith & Nephew TRUCLEAR ULTRA Mini Tissue Removal Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161763
510(k) Type
Traditional
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2016
Days to Decision
148 days
Submission Type
Summary

Smith & Nephew TRUCLEAR ULTRA Mini Tissue Removal Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161763
510(k) Type
Traditional
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2016
Days to Decision
148 days
Submission Type
Summary