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SPINEOLOGY PEEK LUMBAR INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K123652
510(k) Type
Traditional
Applicant
SPINEOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2013
Days to Decision
115 days
Submission Type
Summary

SPINEOLOGY PEEK LUMBAR INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K123652
510(k) Type
Traditional
Applicant
SPINEOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2013
Days to Decision
115 days
Submission Type
Summary