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LEFORTE NEUROSYSTEM BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K091686
510(k) Type
Traditional
Applicant
JEIL MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2009
Days to Decision
157 days
Submission Type
Summary

LEFORTE NEUROSYSTEM BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K091686
510(k) Type
Traditional
Applicant
JEIL MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2009
Days to Decision
157 days
Submission Type
Summary