FDA UDI In Commercial Distribution 🇺🇸 United States

Fusion Posterior Instrument Set

DI: 00191083026077 · Model: 723-416 · Rti Surgical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Fusion Posterior Instrument Set
Primary DI
00191083026077
Version / Model
723-416
Catalog Number
723-416
Company Name
Rti Surgical, Inc.
Labeler DUNS
117560455
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-25
Public Version
5
Public Version Date
2023-10-19
Public Version Status
Update
Public Device Record Key
5e64b5d7-1e09-42b8-8858-27a19f193872

Device Description

FUSION, BONE GRAFT FUNNEL, PLUNGER

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
47872 Bone graft funnel

Identifiers

Type ID
Primary 00191083026077

Customer Contacts