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Keos Lumbar IBFD

Page Type
Cleared 510(K)
510(k) Number
K193174
510(k) Type
Special
Applicant
Keos
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2019
Days to Decision
28 days
Submission Type
Summary

Keos Lumbar IBFD

Page Type
Cleared 510(K)
510(k) Number
K193174
510(k) Type
Special
Applicant
Keos
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2019
Days to Decision
28 days
Submission Type
Summary