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LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002

Page Type
Cleared 510(K)
510(k) Number
K082194
510(k) Type
Traditional
Applicant
LAURIMED LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2008
Days to Decision
24 days
Submission Type
Summary

LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002

Page Type
Cleared 510(K)
510(k) Number
K082194
510(k) Type
Traditional
Applicant
LAURIMED LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2008
Days to Decision
24 days
Submission Type
Summary