Last synced on 20 December 2024 at 11:05 pm

2.1 x 255mm Drill, 22mm Stop

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213072
510(k) Type
Traditional
Applicant
Biomet Micofixation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2022
Days to Decision
334 days
Submission Type
Summary

2.1 x 255mm Drill, 22mm Stop

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213072
510(k) Type
Traditional
Applicant
Biomet Micofixation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2022
Days to Decision
334 days
Submission Type
Summary