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Genesys Spine AIS-C Cervical Anchored Interbody System

Page Type
Cleared 510(K)
510(k) Number
K180056
510(k) Type
Traditional
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2018
Days to Decision
79 days
Submission Type
Summary

Genesys Spine AIS-C Cervical Anchored Interbody System

Page Type
Cleared 510(K)
510(k) Number
K180056
510(k) Type
Traditional
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2018
Days to Decision
79 days
Submission Type
Summary