FDA UDI In Commercial Distribution 🇺🇸 United States

K2M General Instruments

DI: 10888857579675 · Model: PRO-1381 · VB Spine LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
K2M General Instruments
Primary DI
10888857579675
Version / Model
PRO-1381
Catalog Number
PRO-1381
Company Name
VB Spine LLC
Labeler DUNS
119508156
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-24
Public Version
2
Public Version Date
2026-04-20
Public Version Status
Update
Public Device Record Key
b11a7d5d-835a-40c1-852e-3164f0288f95

Device Description

Plate Holder

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
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
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 10888857579675

Customer Contacts