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IMPLEX CONTINUUM KNEE UNITY TIBIAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K980637
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1998
Days to Decision
300 days
Submission Type
Summary

IMPLEX CONTINUUM KNEE UNITY TIBIAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K980637
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1998
Days to Decision
300 days
Submission Type
Summary