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Keos Lumbar IBFD

Page Type
Cleared 510(K)
510(k) Number
K160631
510(k) Type
Traditional
Applicant
KEOS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2016
Days to Decision
130 days
Submission Type
Summary

Keos Lumbar IBFD

Page Type
Cleared 510(K)
510(k) Number
K160631
510(k) Type
Traditional
Applicant
KEOS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2016
Days to Decision
130 days
Submission Type
Summary