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NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) System

Page Type
Cleared 510(K)
510(k) Number
K203129
510(k) Type
Traditional
Applicant
Precision Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2021
Days to Decision
85 days
Submission Type
Summary

NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) System

Page Type
Cleared 510(K)
510(k) Number
K203129
510(k) Type
Traditional
Applicant
Precision Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2021
Days to Decision
85 days
Submission Type
Summary