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Ins Hilden Humeral Arzzt, Ins Hilden Cannulated Tibial Arzzt, Ins Hilden Femoral Arzzt & Ins Hilden Retrograde Femoral Arzzt

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172189
510(k) Type
Traditional
Applicant
Truemed Group LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2018
Days to Decision
180 days
Submission Type
Summary

Ins Hilden Humeral Arzzt, Ins Hilden Cannulated Tibial Arzzt, Ins Hilden Femoral Arzzt & Ins Hilden Retrograde Femoral Arzzt

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172189
510(k) Type
Traditional
Applicant
Truemed Group LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2018
Days to Decision
180 days
Submission Type
Summary