Last synced on 14 November 2025 at 11:06 pm

LEFORTE SYSTEM BONE PLATE

Page Type
Cleared 510(K)
510(k) Number
K091679
510(k) Type
Traditional
Applicant
JEIL MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2009
Days to Decision
115 days
Submission Type
Summary

LEFORTE SYSTEM BONE PLATE

Page Type
Cleared 510(K)
510(k) Number
K091679
510(k) Type
Traditional
Applicant
JEIL MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2009
Days to Decision
115 days
Submission Type
Summary