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Paeon Anterior Cervical Plate System, Elatus Lumbar Plate System

Page Type
Cleared 510(K)
510(k) Number
K223719
510(k) Type
Special
Applicant
Aegis Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2023
Days to Decision
30 days
Submission Type
Summary

Paeon Anterior Cervical Plate System, Elatus Lumbar Plate System

Page Type
Cleared 510(K)
510(k) Number
K223719
510(k) Type
Special
Applicant
Aegis Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2023
Days to Decision
30 days
Submission Type
Summary