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ARENA-C TIFUSE CERVICAL INTERVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141333
510(k) Type
Traditional
Applicant
SPINEFRONTIER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2014
Days to Decision
188 days
Submission Type
Summary

ARENA-C TIFUSE CERVICAL INTERVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141333
510(k) Type
Traditional
Applicant
SPINEFRONTIER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2014
Days to Decision
188 days
Submission Type
Summary