Last synced on 14 November 2025 at 11:06 pm

DEPUY SYNTHES TOMOFIX OSTEOTOMY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K141796
510(k) Type
Traditional
Applicant
SYNTHES (USA) PRODUCTS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2014
Days to Decision
57 days
Submission Type
Summary

DEPUY SYNTHES TOMOFIX OSTEOTOMY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K141796
510(k) Type
Traditional
Applicant
SYNTHES (USA) PRODUCTS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2014
Days to Decision
57 days
Submission Type
Summary