FDA UDI In Commercial Distribution 🇺🇸 United States

Core Lumbar Fixation System

DI: 00840967194257 · Model: 81285-335 · ALPHATEC SPINE, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Core Lumbar Fixation System
Primary DI
00840967194257
Version / Model
81285-335
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-23
Public Version
1
Public Version Date
2020-07-31
Public Version Status
New
Public Device Record Key
0dd5962e-e5e2-49fd-8251-e6a2628f1e09

Device Description

TI STANDARD PEDICLE BOLT - 8.5mm X 35mm

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MNI Orthosis, spinal pedicle fixation
MNH Orthosis, spondylolisthesis spinal fixation

GMDN Terms

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

Identifiers

Type ID
Primary 00840967194257

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K090228 000

Device Sizes

Type Value Unit Text
Length 35 Millimeter
Outer Diameter 8.5 Millimeter