Last synced on 14 November 2025 at 11:06 pm

SYNTHES (USA) MEDIUM EXTERNAL FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K011034
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2001
Days to Decision
83 days
Submission Type
Summary

SYNTHES (USA) MEDIUM EXTERNAL FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K011034
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2001
Days to Decision
83 days
Submission Type
Summary