FDA UDI In Commercial Distribution 🇺🇸 United States

ReLine

DI: 00887517049360 · Model: 10255116P · Nuvasive, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ReLine
Primary DI
00887517049360
Version / Model
10255116P
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
1a70e0c7-b429-40e1-b0f8-3b3f2a533779

Device Description

RSS Iliac Saddle, 5.5mm Straight Ø16

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
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

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

GMDN Terms

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

Identifiers

Type ID
Primary 00887517049360

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K190636 000