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OPTILOCK PERIARTICULAR PLATING

Page Type
Cleared 510(K)
510(k) Number
K092078
510(k) Type
Special
Applicant
BIOMET TRAUMA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2009
Days to Decision
27 days
Submission Type
Summary

OPTILOCK PERIARTICULAR PLATING

Page Type
Cleared 510(K)
510(k) Number
K092078
510(k) Type
Special
Applicant
BIOMET TRAUMA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2009
Days to Decision
27 days
Submission Type
Summary