Last synced on 14 November 2025 at 11:06 pm

AUTOBONE

Page Type
Cleared 510(K)
510(k) Number
K031871
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS EUROPE
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/20/2003
Days to Decision
3 days
Submission Type
Summary

AUTOBONE

Page Type
Cleared 510(K)
510(k) Number
K031871
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS EUROPE
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/20/2003
Days to Decision
3 days
Submission Type
Summary