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TWINFIX FT PK

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072785
510(k) Type
Traditional
Applicant
Smith & Nephew Inc., Endoscopy Division
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2007
Days to Decision
70 days
Submission Type
Summary

TWINFIX FT PK

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072785
510(k) Type
Traditional
Applicant
Smith & Nephew Inc., Endoscopy Division
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2007
Days to Decision
70 days
Submission Type
Summary