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Lucent Intervertebral Body Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K152011
510(k) Type
Traditional
Applicant
Spinal Elements Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/2016
Days to Decision
324 days
Submission Type
Summary

Lucent Intervertebral Body Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K152011
510(k) Type
Traditional
Applicant
Spinal Elements Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/9/2016
Days to Decision
324 days
Submission Type
Summary