FDA UDI In Commercial Distribution 🇺🇸 United States

Valencia Pedicle Screw System

DI: B41797085801 · Model: 970-8580 · 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
B41797085801
Version / Model
970-8580
Company Name
Altus Spine, LLC
Labeler DUNS
078331322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-06
Public Version
1
Public Version Date
2018-04-06
Public Version Status
New
Public Device Record Key
7676546c-3142-4b02-b318-32e9a9c307a1

Device Description

8.5mm x 80mm 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
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MNH Orthosis, spondylolisthesis spinal fixation
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
MNI ORTHOSIS, SPINAL PEDICLE FIXATION

GMDN Terms

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

Identifiers

Type ID
Primary B41797085801
Secondary 00843210114712

Customer Contacts

Device Sizes

Type Value Unit Text
Length 80 Millimeter
Outer Diameter 8.5 Millimeter