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VERTEBRAL SPACER

Page Type
Cleared 510(K)
510(k) Number
K011037
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2002
Days to Decision
452 days
Submission Type
Summary

VERTEBRAL SPACER

Page Type
Cleared 510(K)
510(k) Number
K011037
510(k) Type
Traditional
Applicant
Synthes (Usa)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2002
Days to Decision
452 days
Submission Type
Summary