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The Octane Straight Intervertebral Fusion Device, Ti Coated

Page Type
Cleared 510(K)
510(k) Number
K150152
510(k) Type
Traditional
Applicant
EXACTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2015
Days to Decision
108 days
Submission Type
Summary

The Octane Straight Intervertebral Fusion Device, Ti Coated

Page Type
Cleared 510(K)
510(k) Number
K150152
510(k) Type
Traditional
Applicant
EXACTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/2015
Days to Decision
108 days
Submission Type
Summary