Last synced on 20 January 2023 at 11:05 pm

AOI CRANIAL HELMET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103362
510(k) Type
Traditional
Applicant
ADVANCED ORTHOPRO INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2011
Days to Decision
152 days
Submission Type
Summary

AOI CRANIAL HELMET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103362
510(k) Type
Traditional
Applicant
ADVANCED ORTHOPRO INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2011
Days to Decision
152 days
Submission Type
Summary