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MODIFICATION TO ISKD (INTRAMEDULLARY SKELETAL KINETIC DISTRACTOR)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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