Last synced on 25 April 2025 at 11:05 pm

Halis™ Lumbar Cage System, Lydia™ Anterior Lumbar Fusion System, Dica™ Direction Changeable Lumbar Cage System, KEYSTONE Cage System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230872
510(k) Type
Traditional
Applicant
Shanghai Sanyou Medical Co, LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/12/2023
Days to Decision
257 days
Submission Type
Summary

Halis™ Lumbar Cage System, Lydia™ Anterior Lumbar Fusion System, Dica™ Direction Changeable Lumbar Cage System, KEYSTONE Cage System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230872
510(k) Type
Traditional
Applicant
Shanghai Sanyou Medical Co, LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/12/2023
Days to Decision
257 days
Submission Type
Summary