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CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072537
510(k) Type
Traditional
Applicant
CREASPINE SAS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2007
Days to Decision
99 days
Submission Type
Summary

CREASPINE SUPSTANCE VERTEBRAL BODY REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072537
510(k) Type
Traditional
Applicant
CREASPINE SAS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2007
Days to Decision
99 days
Submission Type
Summary