FDA UDI In Commercial Distribution 🇺🇸 United States

SpheRx

DI: 00887517460875 · Model: 7276545 · Nuvasive, Inc.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SpheRx
Primary DI
00887517460875
Version / Model
7276545
Company Name
Nuvasive, Inc.
Labeler DUNS
053950783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-04
Public Version
1
Public Version Date
2019-12-12
Public Version Status
New
Public Device Record Key
d9b0374e-76c4-41a3-8e0b-9e0f7465cff5

Device Description

SpheRx DBR II Screw, 6.5x45mm Cann Poly

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

GMDN Terms

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

Identifiers

Type ID
Primary 00887517460875

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K083028 000