Last synced on 25 April 2025 at 11:05 pm

Posterior Cervical Spine System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233078
510(k) Type
Traditional
Applicant
Double Medical Technology Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/22/2023
Days to Decision
58 days
Submission Type
Summary

Posterior Cervical Spine System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233078
510(k) Type
Traditional
Applicant
Double Medical Technology Inc.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/22/2023
Days to Decision
58 days
Submission Type
Summary