Last synced on 14 November 2025 at 11:06 pm

VU CPOD INTERVERTEBRAL BODU FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K101363
510(k) Type
Traditional
Applicant
MUSCULOSKELETAL CLINICAL REGULATORY ADVISERS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2010
Days to Decision
216 days
Submission Type
Summary

VU CPOD INTERVERTEBRAL BODU FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K101363
510(k) Type
Traditional
Applicant
MUSCULOSKELETAL CLINICAL REGULATORY ADVISERS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2010
Days to Decision
216 days
Submission Type
Summary