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APEX SPINE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110906
510(k) Type
Traditional
Applicant
Spinecraft, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2011
Days to Decision
117 days
Submission Type
Summary

APEX SPINE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110906
510(k) Type
Traditional
Applicant
Spinecraft, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2011
Days to Decision
117 days
Submission Type
Summary