Last synced on 30 September 2022 at 11:05 pm

Portex® Lancet Point Spinal Needles with NRFit™ connectors, Portex® Pencil Point Spinal Needles with NRFit™ connectors

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172800
510(k) Type
Traditional
Applicant
Smiths Medical ASD, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2018
Days to Decision
269 days
Submission Type
Summary

Portex® Lancet Point Spinal Needles with NRFit™ connectors, Portex® Pencil Point Spinal Needles with NRFit™ connectors

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172800
510(k) Type
Traditional
Applicant
Smiths Medical ASD, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/2018
Days to Decision
269 days
Submission Type
Summary