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BIOMET BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K964970
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/1997
Days to Decision
112 days
Submission Type
Summary

BIOMET BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K964970
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/1997
Days to Decision
112 days
Submission Type
Summary