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NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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