Last synced on 18 April 2025 at 11:05 pm

STRYKER LEIBINGER UNIVERSAL DISTAL RADIUS SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040022
510(k) Type
Traditional
Applicant
STRYKER LEIBINGER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2004
Days to Decision
65 days
Submission Type
Summary

STRYKER LEIBINGER UNIVERSAL DISTAL RADIUS SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040022
510(k) Type
Traditional
Applicant
STRYKER LEIBINGER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2004
Days to Decision
65 days
Submission Type
Summary