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STRYKER TITANIUM CROSS-SCREW SYSTEM, MODEL 234-500-1XX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011319
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2001
Days to Decision
80 days
Submission Type
Summary

STRYKER TITANIUM CROSS-SCREW SYSTEM, MODEL 234-500-1XX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011319
510(k) Type
Traditional
Applicant
Stryker Endoscopy
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2001
Days to Decision
80 days
Submission Type
Summary