FDA UDI In Commercial Distribution 🇺🇸 United States

CoLink® NeoFuse

DI: 00810021865058 · Model: P02 N0081 · IN2BONES USA, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CoLink® NeoFuse
Primary DI
00810021865058
Version / Model
P02 N0081
Company Name
IN2BONES USA, LLC
Labeler DUNS
079700711
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-01-21
Public Version
1
Public Version Date
2022-01-31
Public Version Status
New
Public Device Record Key
d6aa3525-6a02-45c3-af8c-0b13fa45ec9a

Device Description

TARGETING GUIDE, ANTERO-LATERAL, RIGHT

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
FZX Guide, Surgical, Instrument

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 00810021865058

Premarket Submissions

Submission Number Supplement Number
K213069 000