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Kalitec Navigated Instrument System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232572
510(k) Type
Traditional
Applicant
Kalitec Direct, LLC doing business as Kalitec Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2023
Days to Decision
111 days
Submission Type
Summary

Kalitec Navigated Instrument System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232572
510(k) Type
Traditional
Applicant
Kalitec Direct, LLC doing business as Kalitec Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2023
Days to Decision
111 days
Submission Type
Summary