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SureMAX-SA Cervical Standalone System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211111
510(k) Type
Traditional
Applicant
Additive Implants, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2021
Days to Decision
93 days
Submission Type
Summary

SureMAX-SA Cervical Standalone System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211111
510(k) Type
Traditional
Applicant
Additive Implants, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2021
Days to Decision
93 days
Submission Type
Summary