Last synced on 18 April 2025 at 11:05 pm

SMART SCREW ACL MODELS 237020, 237025, 237030, 238020, 238025, 238030, 239020, 239025, 239030

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993073
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, LTD.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
12/6/1999
Days to Decision
83 days
Submission Type
Summary

SMART SCREW ACL MODELS 237020, 237025, 237030, 238020, 238025, 238030, 239020, 239025, 239030

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993073
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, LTD.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
12/6/1999
Days to Decision
83 days
Submission Type
Summary