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SPINEOLGY PEEK BULLET LUMBER INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K111880
510(k) Type
Traditional
Applicant
Spineology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2011
Days to Decision
87 days
Submission Type
Summary

SPINEOLGY PEEK BULLET LUMBER INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K111880
510(k) Type
Traditional
Applicant
Spineology Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2011
Days to Decision
87 days
Submission Type
Summary