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BONE MULCH SCREW

Page Type
Cleared 510(K)
510(k) Number
K941941
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
2/2/1995
Days to Decision
287 days
Submission Type
Summary

BONE MULCH SCREW

Page Type
Cleared 510(K)
510(k) Number
K941941
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
2/2/1995
Days to Decision
287 days
Submission Type
Summary