Last synced on 20 December 2024 at 11:05 pm

STRYKER NAVIGATION SYSTEM-KNEE MODULE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010204
510(k) Type
Traditional
Applicant
STRYKER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2001
Days to Decision
220 days
Submission Type
Summary

STRYKER NAVIGATION SYSTEM-KNEE MODULE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010204
510(k) Type
Traditional
Applicant
STRYKER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2001
Days to Decision
220 days
Submission Type
Summary