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

Page Type
Cleared 510(K)
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)
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