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VERTEBRON PSS PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K033352
510(k) Type
Traditional
Applicant
VERTEBRON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2004
Days to Decision
128 days
Submission Type
Summary

VERTEBRON PSS PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K033352
510(k) Type
Traditional
Applicant
VERTEBRON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2004
Days to Decision
128 days
Submission Type
Summary