FDA UDI In Commercial Distribution 🇺🇸 United States

RADIUS

DI: 07613154514557 · Model: 486613240 · Stryker Corporation
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RADIUS
Primary DI
07613154514557
Version / Model
486613240
Catalog Number
486613240
Company Name
Stryker Corporation
Labeler DUNS
149183167
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-12-08
Public Version
6
Public Version Date
2023-07-10
Public Version Status
Update
Public Device Record Key
64eb8176-ccda-4ce8-91ea-7a40f6078df1

Device Description

TITANIUM SPINAL ROD, WITH HEX

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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
MNH Orthosis, spondylolisthesis spinal fixation
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
OSH Pedicle screw spinal system, adolescent idiopathic scoliosis
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

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

Identifiers

Type ID
Primary 07613154514557

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 5.5 Millimeter
Length 240.0 Millimeter