Last synced on 14 November 2025 at 11:06 pm

IMPLEX HEP ACETABULAR REVISION CUP, CEMENTED OR CEMENTLESS MODEL A-240 SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980486
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1998
Days to Decision
64 days
Submission Type
Summary

IMPLEX HEP ACETABULAR REVISION CUP, CEMENTED OR CEMENTLESS MODEL A-240 SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980486
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1998
Days to Decision
64 days
Submission Type
Summary