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Atlas Spine Lateral Expandable Interbody System

Page Type
Cleared 510(K)
510(k) Number
K243191
510(k) Type
Traditional
Applicant
Atlas Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2024
Days to Decision
57 days
Submission Type
Statement

Atlas Spine Lateral Expandable Interbody System

Page Type
Cleared 510(K)
510(k) Number
K243191
510(k) Type
Traditional
Applicant
Atlas Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2024
Days to Decision
57 days
Submission Type
Statement