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CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K102339
510(k) Type
Traditional
Applicant
CONMED LINVATEC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2010
Days to Decision
97 days
Submission Type
Summary

CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K102339
510(k) Type
Traditional
Applicant
CONMED LINVATEC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2010
Days to Decision
97 days
Submission Type
Summary