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aprevo Intervertebral Body Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K202034
510(k) Type
Traditional
Applicant
Carlsmed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2020
Days to Decision
133 days
Submission Type
Summary

aprevo Intervertebral Body Fusion Device

Page Type
Cleared 510(K)
510(k) Number
K202034
510(k) Type
Traditional
Applicant
Carlsmed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2020
Days to Decision
133 days
Submission Type
Summary