Last synced on 14 June 2024 at 11:05 pm

STRYKER CUSTOM TI IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052871
510(k) Type
Traditional
Applicant
STRYKER LEIBINGER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2005
Days to Decision
66 days
Submission Type
Summary

STRYKER CUSTOM TI IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052871
510(k) Type
Traditional
Applicant
STRYKER LEIBINGER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2005
Days to Decision
66 days
Submission Type
Summary