FDA UDI In Commercial Distribution 🇺🇸 United States

MaxFuse PEEK VBR SYSTEM

DI: 00191083015804 · Model: 724-903 · Rti Surgical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MaxFuse PEEK VBR SYSTEM
Primary DI
00191083015804
Version / Model
724-903
Catalog Number
724-903
Company Name
Rti Surgical, Inc.
Labeler DUNS
117560455
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-04
Public Version
5
Public Version Date
2023-10-19
Public Version Status
Update
Public Device Record Key
9d5ce302-c69c-4d38-9a53-066c0a707ac4

Device Description

MAXFUSE, 12x14x4446 REPLICA TRL SPACER

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
HWT TEMPLATE

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Primary 00191083015804
Previous 00191083028590

Customer Contacts