Last synced on 14 November 2025 at 11:06 pm

SYNTHES ANTEGRA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063158
510(k) Type
Special
Applicant
SYNTHES SPINE CO.LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2006
Days to Decision
28 days
Submission Type
Summary

SYNTHES ANTEGRA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063158
510(k) Type
Special
Applicant
SYNTHES SPINE CO.LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2006
Days to Decision
28 days
Submission Type
Summary