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SYNTHES HINDFOOT ARTHRODESIS NAIL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K051678
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2005
Days to Decision
90 days
Submission Type
Summary

SYNTHES HINDFOOT ARTHRODESIS NAIL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K051678
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/2005
Days to Decision
90 days
Submission Type
Summary