Last synced on 25 April 2025 at 11:05 pm

FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, and BALTEUM™ & BALTEUM-ONE™ Lumbar Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222572
510(k) Type
Traditional
Applicant
Dio Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2022
Days to Decision
54 days
Submission Type
Summary

FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, and BALTEUM™ & BALTEUM-ONE™ Lumbar Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222572
510(k) Type
Traditional
Applicant
Dio Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2022
Days to Decision
54 days
Submission Type
Summary