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SeaSpine® Shoreline™ ACS- Anterior Cervical Standalone System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190655
510(k) Type
Traditional
Applicant
SeaSpine Orthopedics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2019
Days to Decision
46 days
Submission Type
Summary

SeaSpine® Shoreline™ ACS- Anterior Cervical Standalone System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190655
510(k) Type
Traditional
Applicant
SeaSpine Orthopedics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2019
Days to Decision
46 days
Submission Type
Summary