FDA UDI In Commercial Distribution 🇺🇸 United States

MESA® Spinal System

DI: 10888857136830 · Model: 801-07545 · K2M, INC.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MESA® Spinal System
Primary DI
10888857136830
Version / Model
801-07545
Catalog Number
801-07545
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2023-09-19
Public Version Status
Update
Public Device Record Key
19cabec6-93fb-494a-878a-577659a3d42c

Device Description

Polyaxial 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
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
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
OSH Pedicle screw spinal system, adolescent idiopathic scoliosis
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MNH Orthosis, spondylolisthesis spinal fixation

GMDN Terms

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

Identifiers

Type ID
Primary 10888857136830

Customer Contacts

Device Sizes

Type Value Unit Text
Length 45 Millimeter
Outer Diameter 7.5 Millimeter