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LACTOSORB MENISCAL SCREW

Page Type
Cleared 510(K)
510(k) Number
K002020
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2000
Days to Decision
53 days
Submission Type
Summary

LACTOSORB MENISCAL SCREW

Page Type
Cleared 510(K)
510(k) Number
K002020
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2000
Days to Decision
53 days
Submission Type
Summary