Last synced on 30 November 2024 at 11:09 am

Synxess Neurovascular Guidewire

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240871
510(k) Type
Traditional
Applicant
Enlight Medical Technologies (Shenzhen) Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/18/2024
Days to Decision
234 days
Submission Type
Summary

Synxess Neurovascular Guidewire

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240871
510(k) Type
Traditional
Applicant
Enlight Medical Technologies (Shenzhen) Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/18/2024
Days to Decision
234 days
Submission Type
Summary