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SPINEOLOGY PEEK LUMBAR INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K121129
510(k) Type
Special
Applicant
SPINEOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2012
Days to Decision
61 days
Submission Type
Summary

SPINEOLOGY PEEK LUMBAR INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K121129
510(k) Type
Special
Applicant
SPINEOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2012
Days to Decision
61 days
Submission Type
Summary