FDA UDI In Commercial Distribution 🇺🇸 United States

VuePoint

DI: 00887517399113 · Model: 8975512 · Nuvasive, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VuePoint
Primary DI
00887517399113
Version / Model
8975512
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
f560ce99-aa66-4ebc-8343-5f684be0ca21

Device Description

VuePoint® II Screw, 3.5x12mm FA

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

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

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00887517399113

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K093319 000
K150474 000