Last synced on 2 May 2025 at 11:05 pm

IMPLEX A-230 POROUS ACETABULAR CUP SYST. CEMENTED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932924
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/1994
Days to Decision
331 days
Submission Type
Statement

IMPLEX A-230 POROUS ACETABULAR CUP SYST. CEMENTED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932924
510(k) Type
Traditional
Applicant
IMPLEX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/1994
Days to Decision
331 days
Submission Type
Statement