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LAURIMED SPINAL INJECTION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080140
510(k) Type
Traditional
Applicant
LAURIMED LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2008
Days to Decision
108 days
Submission Type
Summary

LAURIMED SPINAL INJECTION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080140
510(k) Type
Traditional
Applicant
LAURIMED LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2008
Days to Decision
108 days
Submission Type
Summary