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INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K110045
510(k) Type
Special
Applicant
VERTEBRAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/2011
Days to Decision
28 days
Submission Type
Summary

INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K110045
510(k) Type
Special
Applicant
VERTEBRAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/2011
Days to Decision
28 days
Submission Type
Summary