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LACTOSORB HAND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K991763
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1999
Days to Decision
67 days
Submission Type
Summary

LACTOSORB HAND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K991763
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1999
Days to Decision
67 days
Submission Type
Summary