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MODIFICATION TO STEATHSTATION TREATMENT GUIDANCE PLATFORM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001153
510(k) Type
Special
Applicant
Medtronic Surgical Navigation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2000
Days to Decision
23 days
Submission Type
Summary

MODIFICATION TO STEATHSTATION TREATMENT GUIDANCE PLATFORM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001153
510(k) Type
Special
Applicant
Medtronic Surgical Navigation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2000
Days to Decision
23 days
Submission Type
Summary