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NEUROSCOUT STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100351
510(k) Type
Special
Applicant
Codman & Shurtleff, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2010
Days to Decision
32 days
Submission Type
Summary

NEUROSCOUT STEERABLE GUIDEWIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100351
510(k) Type
Special
Applicant
Codman & Shurtleff, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2010
Days to Decision
32 days
Submission Type
Summary