Last synced on 14 November 2025 at 11:06 pm

MODIFICATION TO ISKD (INTRAMEDULLARY SKELETAL KINETIC DISTRACTOR)

Page Type
Cleared 510(K)
510(k) Number
K031219
510(k) Type
Special
Applicant
ORTHOFIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/2003
Days to Decision
41 days
Submission Type
Summary

MODIFICATION TO ISKD (INTRAMEDULLARY SKELETAL KINETIC DISTRACTOR)

Page Type
Cleared 510(K)
510(k) Number
K031219
510(k) Type
Special
Applicant
ORTHOFIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/2003
Days to Decision
41 days
Submission Type
Summary