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Reprocessed Stryker External Fixation Devices

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153415
510(k) Type
Special
Applicant
Stryker Sustainability Solutions
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2016
Days to Decision
49 days
Submission Type
Summary

Reprocessed Stryker External Fixation Devices

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153415
510(k) Type
Special
Applicant
Stryker Sustainability Solutions
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2016
Days to Decision
49 days
Submission Type
Summary