Last synced on 20 January 2023 at 11:05 pm

Codman Certas Plus Electronic Tool Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181902
510(k) Type
Traditional
Applicant
Integra LifeSciences Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2018
Days to Decision
101 days
Submission Type
Summary

Codman Certas Plus Electronic Tool Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181902
510(k) Type
Traditional
Applicant
Integra LifeSciences Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2018
Days to Decision
101 days
Submission Type
Summary