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LACTOSORB MENISCAL REPAIR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K982095
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/1999
Days to Decision
226 days
Submission Type
Summary

LACTOSORB MENISCAL REPAIR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K982095
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/1999
Days to Decision
226 days
Submission Type
Summary