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HERNIATOME PERCUTANEOUS DISECTOMY DEVICE - CERVICAL, HERNIATOME PERCUTANEOUS DISECTOMY DEVICE - LUMBAR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141557
510(k) Type
Traditional
Applicant
Gallini Medical Devices, Srl
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2014
Days to Decision
179 days
Submission Type
Summary

HERNIATOME PERCUTANEOUS DISECTOMY DEVICE - CERVICAL, HERNIATOME PERCUTANEOUS DISECTOMY DEVICE - LUMBAR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141557
510(k) Type
Traditional
Applicant
Gallini Medical Devices, Srl
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2014
Days to Decision
179 days
Submission Type
Summary