Last synced on 25 January 2026 at 3:41 am

OSTEO ACL SCREW MODEL;237020T, 237025T, 237030T, 238020T, 238025T, 238030T, 239020T, 239025T, 239030T, 231020T, 231025T,

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032894
510(k) Type
Traditional
Applicant
Linvatec Biomaterials, Inc.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
5/7/2004
Days to Decision
233 days
Submission Type
Summary

OSTEO ACL SCREW MODEL;237020T, 237025T, 237030T, 238020T, 238025T, 238030T, 239020T, 239025T, 239030T, 231020T, 231025T,

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032894
510(k) Type
Traditional
Applicant
Linvatec Biomaterials, Inc.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
5/7/2004
Days to Decision
233 days
Submission Type
Summary