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SURESHOT Distal Targeting System V4.0 Trauma Interface

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170977
510(k) Type
Special
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2017
Days to Decision
30 days
Submission Type
Summary

SURESHOT Distal Targeting System V4.0 Trauma Interface

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170977
510(k) Type
Special
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2017
Days to Decision
30 days
Submission Type
Summary