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TI. ALLOY 2.0 MM CORTEX SCREW

Page Type
Cleared 510(K)
510(k) Number
K952272
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/1995
Days to Decision
77 days
Submission Type
Summary

TI. ALLOY 2.0 MM CORTEX SCREW

Page Type
Cleared 510(K)
510(k) Number
K952272
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/1995
Days to Decision
77 days
Submission Type
Summary