FDA UDI In Commercial Distribution 🇺🇸 United States

VuePoint

DI: 00887517954268 · Model: 8976141P · Nuvasive, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VuePoint
Primary DI
00887517954268
Version / Model
8976141P
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-30
Public Version
1
Public Version Date
2018-08-30
Public Version Status
New
Public Device Record Key
7366e7d4-c670-4b0d-8583-4138ee1459c0

Device Description

VuePoint II Ti Rod, Ø3.5x110mm Curved

Device Characteristics

Single Use
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NKG Orthosis, cervical pedicle screw spinal fixation
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00887517954268

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K180198 000