Last synced on 25 January 2026 at 3:41 am

UNIVERSAL ACETABULAR COMPONENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861433
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/27/1986
Days to Decision
194 days

UNIVERSAL ACETABULAR COMPONENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861433
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/27/1986
Days to Decision
194 days