FDA UDI In Commercial Distribution 🇺🇸 United States

CAYMAN Plate System

DI: 10888857019652 · Model: 1208-90010 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CAYMAN Plate System
Primary DI
10888857019652
Version / Model
1208-90010
Catalog Number
1208-90010
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-24
Public Version
1
Public Version Date
2022-07-04
Public Version Status
New
Public Device Record Key
ca9b63bb-62aa-41ca-aba2-14f6d5127595

Device Description

Temporary Fixation Pin, Threaded

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
Yes
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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
61300 Internal spinal fixation procedure kit, single-use

Identifiers

Type ID
Primary 10888857019652

Customer Contacts