FDA UDI In Commercial Distribution 🇺🇸 United States

Valencia Pedicle Screw System

DI: B41797045501 · Model: 970-4550 · Altus Spine, LLC
Product Codes
5
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Valencia Pedicle Screw System
Primary DI
B41797045501
Version / Model
970-4550
Company Name
Altus Spine, LLC
Labeler DUNS
078331322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-28
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
a744164d-1116-436b-8c27-56b681eb6eae

Device Description

4.5mm x 50mm Solid Dual Lead Multi-Axial Screw

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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MNH Orthosis, spondylolisthesis spinal fixation
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

GMDN Terms

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

Identifiers

Type ID
Primary B41797045501
Secondary 00843210114323

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 4.5 Millimeter
Length 50 Millimeter