Last synced on 18 April 2025 at 11:05 pm

23 MM SINGLE-PEG PATELLA COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061340
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2006
Days to Decision
133 days
Submission Type
Summary

23 MM SINGLE-PEG PATELLA COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061340
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2006
Days to Decision
133 days
Submission Type
Summary