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E-SP COMBINED EPI SPINAL MINISET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925014
510(k) Type
Traditional
Applicant
NEURO TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
4/19/1993
Days to Decision
199 days
Submission Type
Statement

E-SP COMBINED EPI SPINAL MINISET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925014
510(k) Type
Traditional
Applicant
NEURO TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
4/19/1993
Days to Decision
199 days
Submission Type
Statement