FDA UDI In Commercial Distribution 🇺🇸 United States

NVM5

DI: 00887517168634 · Model: 2021003 · Nuvasive, Inc.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NVM5
Primary DI
00887517168634
Version / Model
2021003
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-26
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
9ffd7585-7324-4c99-878f-780d5310d515

Device Description

NV Next Generation Patient Mod

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OLO Orthopedic stereotaxic instrument
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE
IKN Electromyograph, diagnostic
HAW Neurological stereotaxic Instrument
PDQ Neurosurgical nerve locator
ETN STIMULATOR, NERVE

GMDN Terms

Code Name
46566 Neurophysiologic monitoring system

Identifiers

Type ID
Primary 00887517168634

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K143641 000