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CONTINUUM KNEE SYSTEM COBALT CHROMIUM ALLOY TIBIAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K984291
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/1999
Days to Decision
62 days
Submission Type
Summary

CONTINUUM KNEE SYSTEM COBALT CHROMIUM ALLOY TIBIAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K984291
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/1999
Days to Decision
62 days
Submission Type
Summary