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ENNOVATE Spinal System

Page Type
Cleared 510(K)
510(k) Number
K162134
510(k) Type
Traditional
Applicant
Aesculap Implant Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2016
Days to Decision
135 days
Submission Type
Summary

ENNOVATE Spinal System

Page Type
Cleared 510(K)
510(k) Number
K162134
510(k) Type
Traditional
Applicant
Aesculap Implant Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2016
Days to Decision
135 days
Submission Type
Summary