FDA UDI In Commercial Distribution 🇺🇸 United States

ReLine

DI: 00887517039293 · Model: 13327535P · Nuvasive, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ReLine
Primary DI
00887517039293
Version / Model
13327535P
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-25
Public Version
1
Public Version Date
2021-03-05
Public Version Status
New
Public Device Record Key
dfd5ad7a-38ae-4bd5-94dc-9230ac6cc93d

Device Description

RELINE-O Screw+LS, 7.5x35mm 2S Red

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
Radiation Sterilization

Product Codes

Code Name
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKB Thoracolumbosacral pedicle screw system
PML bone cement, posterior screw augmentation

GMDN Terms

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

Identifiers

Type ID
Primary 00887517039293

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K180498 000