FDA UDI In Commercial Distribution 🇺🇸 United States

Altus Spine HA Pedicle Screw System

DI: 00843210157795 · Model: 822-8590HA · Altus Spine, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Altus Spine HA Pedicle Screw System
Primary DI
00843210157795
Version / Model
822-8590HA
Company Name
Altus Spine, LLC
Labeler DUNS
078331322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-05
Public Version
1
Public Version Date
2023-04-13
Public Version Status
New
Public Device Record Key
918308e1-eadc-469f-89f4-f7621d0c071b

Device Description

Cannulated Polyaxial Pedicle Screw, HA Coated.

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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NKB Thoracolumbosacral Pedicle Screw System
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00843210157795

Premarket Submissions

Submission Number Supplement Number
K200922 000