Last synced on 25 April 2025 at 11:05 pm

ZIRCONIA CERAMIC MODULAR HEADS(TYPE I TAPER) MODIF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913420
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1992
Days to Decision
175 days
Submission Type
Statement

ZIRCONIA CERAMIC MODULAR HEADS(TYPE I TAPER) MODIF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913420
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1992
Days to Decision
175 days
Submission Type
Statement