Last synced on 25 January 2026 at 3:41 am

SMPLE PLATE AND SCREWS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093983
510(k) Type
Traditional
Applicant
Biomet Trauma (Aka Ebi, Lp)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2010
Days to Decision
85 days
Submission Type
Summary

SMPLE PLATE AND SCREWS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093983
510(k) Type
Traditional
Applicant
Biomet Trauma (Aka Ebi, Lp)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/2010
Days to Decision
85 days
Submission Type
Summary