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CONTROLLED DELIVERY FOR OSTEOPLASTY (CDO SYSTEM) AND GRAFT PREPARATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072330
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2007
Days to Decision
108 days
Submission Type
Summary

CONTROLLED DELIVERY FOR OSTEOPLASTY (CDO SYSTEM) AND GRAFT PREPARATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072330
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2007
Days to Decision
108 days
Submission Type
Summary