Last synced on 25 January 2026 at 3:41 am

SMARTWEDGE ACL, MODELS 430623, 430628, 430723, 430728, 430823, 430828

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000616
510(k) Type
Special
Applicant
Bionx Implants, Ltd.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
3/23/2000
Days to Decision
28 days
Submission Type
Summary

SMARTWEDGE ACL, MODELS 430623, 430628, 430723, 430728, 430823, 430828

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000616
510(k) Type
Special
Applicant
Bionx Implants, Ltd.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
3/23/2000
Days to Decision
28 days
Submission Type
Summary