FDA UDI In Commercial Distribution 🇺🇸 United States

Cross-Fuse® II PEEK IBF System

DI: 00191083033280 · Model: 38-INSERTER-HL · Rti Surgical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Cross-Fuse® II PEEK IBF System
Primary DI
00191083033280
Version / Model
38-INSERTER-HL
Catalog Number
38-INSERTER-HL
Company Name
Rti Surgical, Inc.
Labeler DUNS
117560455
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-02
Public Version
4
Public Version Date
2023-10-19
Public Version Status
Update
Public Device Record Key
4b078545-20f8-4a76-852e-dfd3bf30ee08

Device Description

INSERTER

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
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Previous 00846468061128
Primary 00191083033280

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 12 Degrees/18 Degrees