Last synced on 20 December 2024 at 11:05 pm

MODIFICATION TO: INJECTABLE MIMIX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012569
510(k) Type
Special
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2001
Days to Decision
134 days
Submission Type
Summary

MODIFICATION TO: INJECTABLE MIMIX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012569
510(k) Type
Special
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2001
Days to Decision
134 days
Submission Type
Summary