Last synced on 25 January 2026 at 3:41 am

VLP 2.7MM EXTRA LARGE PERCUTANEOUS CALCANEUS PLATE, PERI-LOC 3.5MM ANTERIOR ANKLE FUSION PLATES, PERI-LOC 3.5MM HINDFOOT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120667
510(k) Type
Special
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2012
Days to Decision
30 days
Submission Type
Summary

VLP 2.7MM EXTRA LARGE PERCUTANEOUS CALCANEUS PLATE, PERI-LOC 3.5MM ANTERIOR ANKLE FUSION PLATES, PERI-LOC 3.5MM HINDFOOT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120667
510(k) Type
Special
Applicant
Smith & Nephew, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2012
Days to Decision
30 days
Submission Type
Summary