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MODIFICATION TO UNIVERSAL MULTIAXIS (UNIMAX) PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024313
510(k) Type
Special
Applicant
PISHARODI SURGICALS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2003
Days to Decision
248 days
Submission Type
Summary

MODIFICATION TO UNIVERSAL MULTIAXIS (UNIMAX) PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K024313
510(k) Type
Special
Applicant
PISHARODI SURGICALS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2003
Days to Decision
248 days
Submission Type
Summary