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SPINAL USA ANTERIOR CERVICAL INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K083118
510(k) Type
Traditional
Applicant
SPINAL USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2009
Days to Decision
217 days
Submission Type
Summary

SPINAL USA ANTERIOR CERVICAL INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K083118
510(k) Type
Traditional
Applicant
SPINAL USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2009
Days to Decision
217 days
Submission Type
Summary