Last synced on 23 February 2024 at 11:04 pm

CranioXpand

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230211
510(k) Type
Traditional
Applicant
KLS-Martin L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2023
Days to Decision
299 days
Submission Type
Summary

CranioXpand

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230211
510(k) Type
Traditional
Applicant
KLS-Martin L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2023
Days to Decision
299 days
Submission Type
Summary