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IMPLEX ALUMINA FEMORAL HEAD

Page Type
Cleared 510(K)
510(k) Number
K990183
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1999
Days to Decision
142 days
Submission Type
Summary

IMPLEX ALUMINA FEMORAL HEAD

Page Type
Cleared 510(K)
510(k) Number
K990183
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1999
Days to Decision
142 days
Submission Type
Summary