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MAESTRO WRIST FRACTURE IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K080426
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2008
Days to Decision
160 days
Submission Type
Summary

MAESTRO WRIST FRACTURE IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K080426
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2008
Days to Decision
160 days
Submission Type
Summary