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KHEIRON® Spinal Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211981
510(k) Type
Traditional
Applicant
S.M.A.I.O
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/9/2022
Days to Decision
349 days
Submission Type
Summary

KHEIRON® Spinal Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211981
510(k) Type
Traditional
Applicant
S.M.A.I.O
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/9/2022
Days to Decision
349 days
Submission Type
Summary