FDA UDI In Commercial Distribution 🇺🇸 United States

CHESAPEAKE® Stabilization System

DI: 10888857082076 · Model: 3608-213123 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CHESAPEAKE® Stabilization System
Primary DI
10888857082076
Version / Model
3608-213123
Catalog Number
3608-213123
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-10
Public Version
2
Public Version Date
2023-07-31
Public Version Status
Update
Public Device Record Key
a166d94a-9c33-4752-8d55-ac2dbe0d3687

Device Description

3-Screw Titanium Implant, Size 12x17x13 mm

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
OVE Intervertebral fusion device with integrated fixation, cervical

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 10888857082076

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K111439 000

Device Sizes

Type Value Unit Text
Length 12 Millimeter
Height 13 Millimeter
Width 17 Millimeter
Device Size Text, specify 3 Screw