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VKS/TC-PLUS REVISION KNEE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032215
510(k) Type
Special
Applicant
PLUS ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2003
Days to Decision
18 days
Submission Type
Summary

VKS/TC-PLUS REVISION KNEE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032215
510(k) Type
Special
Applicant
PLUS ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2003
Days to Decision
18 days
Submission Type
Summary