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SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K094002
510(k) Type
Traditional
Applicant
SPARTEK MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2010
Days to Decision
130 days
Submission Type
Summary

SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K094002
510(k) Type
Traditional
Applicant
SPARTEK MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/2010
Days to Decision
130 days
Submission Type
Summary