Last synced on 14 November 2025 at 11:06 pm

VU APOD INTERVERTABRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K080822
510(k) Type
Traditional
Applicant
THEKEN SPINE LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2008
Days to Decision
100 days
Submission Type
Summary

VU APOD INTERVERTABRAL BODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K080822
510(k) Type
Traditional
Applicant
THEKEN SPINE LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2008
Days to Decision
100 days
Submission Type
Summary