Last synced on 14 November 2025 at 11:06 pm

SYNTHES TOMOFIX OSTEOTOMY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K023941
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2003
Days to Decision
58 days
Submission Type
Summary

SYNTHES TOMOFIX OSTEOTOMY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K023941
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2003
Days to Decision
58 days
Submission Type
Summary