FDA UDI In Commercial Distribution 🇺🇸 United States

GMA 2.0 Pedicle Screw System

DI: 00810021380315 · Model: 101-0110-N · GRAFTON MEDICAL ALLIANCE, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GMA 2.0 Pedicle Screw System
Primary DI
00810021380315
Version / Model
101-0110-N
Catalog Number
101-0110-N
Company Name
GRAFTON MEDICAL ALLIANCE, INC.
Labeler DUNS
063381119
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-25
Public Version
2
Public Version Date
2020-01-17
Public Version Status
Update
Public Device Record Key
8aa7592c-fe7d-4788-b53f-662788295aba

Device Description

PRE-BENT ROD, ø5.5 X 110

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
NKB Thoracolumbosacral Pedicle Screw System
MNH Orthosis, Spondylolisthesis Spinal Fixation

GMDN Terms

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

Identifiers

Type ID
Primary 00810021380315

Customer Contacts

Phone
630-568-3061

Premarket Submissions

Submission Number Supplement Number
K133063 000
K192915 000

Device Sizes

Type Value Unit Text
Outer Diameter 5.5 Millimeter
Length 110 Millimeter