FDA UDI In Commercial Distribution 🇺🇸 United States

ReLine

DI: 00887517802446 · Model: 20345120 · Nuvasive, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ReLine
Primary DI
00887517802446
Version / Model
20345120
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-27
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
c41234f7-678a-4f2c-b563-c5437a7144b7

Device Description

RSS Ti Rod, 4.5x120mm Straight

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
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
KWQ Appliance, fixation, spinal intervertebral body
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKB Thoracolumbosacral pedicle screw system

GMDN Terms

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

Identifiers

Type ID
Primary 00887517802446

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K170126 000