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SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM

Page Type
Cleared 510(K)
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)
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