FDA UDI In Commercial Distribution 🇺🇸 United States

3DP Cervical Interbody System

DI: M719GC3RHS090 · Model: 1 · Genesys Orthopedics Systems LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
3DP Cervical Interbody System
Primary DI
M719GC3RHS090
Version / Model
1
Catalog Number
GC3-RH-S09
Company Name
Genesys Orthopedics Systems LLC
Labeler DUNS
017921066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-23
Public Version
2
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
87a6d598-dabe-449f-a768-22f76c1cf26b

Device Description

Small 9mm 3DP Cervical Rasp with Handle

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
OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary M719GC3RHS090

Customer Contacts

Phone
5123817070

Premarket Submissions

Submission Number Supplement Number
K191489 000