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SMITH & NEPHEW PEEK INTERFERENCE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083226
510(k) Type
Traditional
Applicant
Smith & Nephew Endoscopy, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2009
Days to Decision
88 days
Submission Type
Summary

SMITH & NEPHEW PEEK INTERFERENCE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083226
510(k) Type
Traditional
Applicant
Smith & Nephew Endoscopy, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2009
Days to Decision
88 days
Submission Type
Summary