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INTERFUSE INVERTEBRAL BODY FUSION DEVICE MODEL 9076

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093675
510(k) Type
Special
Applicant
Vertebral Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2009
Days to Decision
26 days
Submission Type
Summary

INTERFUSE INVERTEBRAL BODY FUSION DEVICE MODEL 9076

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093675
510(k) Type
Special
Applicant
Vertebral Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2009
Days to Decision
26 days
Submission Type
Summary