Last synced on 30 November 2024 at 11:09 am

MOLDED CRANIAL HELMET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012920
510(k) Type
Traditional
Applicant
FAIRVIEW ORTHOPEDIC LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/2001
Days to Decision
90 days
Submission Type
Summary

MOLDED CRANIAL HELMET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012920
510(k) Type
Traditional
Applicant
FAIRVIEW ORTHOPEDIC LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/2001
Days to Decision
90 days
Submission Type
Summary