FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

NAV PAK Needle, NIM NAV PAK Needle

K Number: K182662 · Decision Apr 10, 2019
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
34
Applicant Total
2
Review Days
197

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Basic Information

Device Name
NAV PAK Needle, NIM NAV PAK Needle
K Number
K182662
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1820
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Boston Endo Surgical Tech,
Date Received
September 25, 2018
Decision Date
April 10, 2019
Product Code
PDQ
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PDQ Neurosurgical Nerve Locator

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PDQ), ordered by most recent decision date.

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Other Clearances by Boston Endo Surgical Tech,

K Number Device Name
K180542 NIM PAK Needle; NIM XPAK Needle; NIM Pedicle Probe