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DUAL TOP ANCHOR SYSTEM SCREWS

Page Type
Cleared 510(K)
510(k) Number
K033767
510(k) Type
Traditional
Applicant
JEIL MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2004
Days to Decision
83 days
Submission Type
Summary

DUAL TOP ANCHOR SYSTEM SCREWS

Page Type
Cleared 510(K)
510(k) Number
K033767
510(k) Type
Traditional
Applicant
JEIL MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2004
Days to Decision
83 days
Submission Type
Summary