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LACTOSORB MINI INTERFERENCE SCREW

Page Type
Cleared 510(K)
510(k) Number
K021254
510(k) Type
Traditional
Applicant
BIOMET ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2002
Days to Decision
89 days
Submission Type
Summary

LACTOSORB MINI INTERFERENCE SCREW

Page Type
Cleared 510(K)
510(k) Number
K021254
510(k) Type
Traditional
Applicant
BIOMET ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2002
Days to Decision
89 days
Submission Type
Summary