FDA UDI In Commercial Distribution 🇺🇸 United States

Orthros

DI: B030CP008360 · Model: CP-008-36 · CAMBER SPINE TECHNOLOGIES, LLC
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Orthros
Primary DI
B030CP008360
Version / Model
CP-008-36
Company Name
CAMBER SPINE TECHNOLOGIES, LLC
Labeler DUNS
054205979
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-04
Public Version
3
Public Version Date
2020-02-05
Public Version Status
Update
Public Device Record Key
53ffa657-70bc-4670-a656-ac8706e97c2b

Device Description

Ø5.5mm Straight Rod, 135mm Lg.

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
KWQ Appliance, Fixation, Spinal Intervertebral Body
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease

GMDN Terms

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

Identifiers

Type ID
Primary B030CP008360

Customer Contacts

Device Sizes

Type Value Unit Text
Length 135 Millimeter
Outer Diameter 5.5 Millimeter