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MODIFIED TO MODULAR FR SEVERE BONE LOSS TRAUMA

Page Type
Cleared 510(K)
510(k) Number
K002324
510(k) Type
Special
Applicant
SULZER MEDICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2000
Days to Decision
24 days
Submission Type
Summary

MODIFIED TO MODULAR FR SEVERE BONE LOSS TRAUMA

Page Type
Cleared 510(K)
510(k) Number
K002324
510(k) Type
Special
Applicant
SULZER MEDICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2000
Days to Decision
24 days
Submission Type
Summary