Last synced on 23 September 2022 at 11:05 pm

CODMAN Hydrocephalus Valves, Catheters & Accessories (Bundled)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172022
510(k) Type
Traditional
Applicant
Codman & Shurtleff, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2017
Days to Decision
90 days
Submission Type
Summary

CODMAN Hydrocephalus Valves, Catheters & Accessories (Bundled)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172022
510(k) Type
Traditional
Applicant
Codman & Shurtleff, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2017
Days to Decision
90 days
Submission Type
Summary