FDA UDI In Commercial Distribution 🇺🇸 United States

CHESAPEAKE® Stabilization System

DI: 10888857026537 · Model: 2008-90153 · K2M, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CHESAPEAKE® Stabilization System
Primary DI
10888857026537
Version / Model
2008-90153
Catalog Number
2008-90153
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
4
Public Version Date
2023-09-08
Public Version Status
Update
Public Device Record Key
603234ba-91b1-4276-9417-6c96ef81d4de

Device Description

Lordotic Trial, Size 30x40x21 mm, 30°

Device Characteristics

Single Use
No
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
OVD Intervertebral fusion device with integrated fixation, lumbar
OVE Intervertebral fusion device with integrated fixation, cervical

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 10888857026537

Customer Contacts

Device Sizes

Type Value Unit Text
Angle 30 degree
Width 40 Millimeter
Length 30 Millimeter
Height 21 Millimeter