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Ayers Rock Cervical interbody fusion system

Page Type
Cleared 510(K)
510(k) Number
K162694
510(k) Type
Traditional
Applicant
Spineway
Country
France
FDA Decision
Substantially Equivalent
Decision Date
1/12/2017
Days to Decision
107 days
Submission Type
Summary

Ayers Rock Cervical interbody fusion system

Page Type
Cleared 510(K)
510(k) Number
K162694
510(k) Type
Traditional
Applicant
Spineway
Country
France
FDA Decision
Substantially Equivalent
Decision Date
1/12/2017
Days to Decision
107 days
Submission Type
Summary