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DePuy Synthes Porous Polyethylene Implants and Titanium Wires Portfolio – MR Conditional

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183472
510(k) Type
Traditional
Applicant
Synthes (USA) Products LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2019
Days to Decision
89 days
Submission Type
Summary

DePuy Synthes Porous Polyethylene Implants and Titanium Wires Portfolio – MR Conditional

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183472
510(k) Type
Traditional
Applicant
Synthes (USA) Products LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2019
Days to Decision
89 days
Submission Type
Summary