Last synced on 25 April 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231460
510(k) Type
Traditional
Applicant
K&J Consulting Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2023
Days to Decision
58 days
Submission Type
Summary

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231460
510(k) Type
Traditional
Applicant
K&J Consulting Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2023
Days to Decision
58 days
Submission Type
Summary