FDA UDI In Commercial Distribution 🇺🇸 United States

OptiMesh Multiplanar Expandable Interbody Fusion System

DI: M7403100010 · Model: 10-01-99 · SPINEOLOGY INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OptiMesh Multiplanar Expandable Interbody Fusion System
Primary DI
M7403100010
Version / Model
10-01-99
Catalog Number
310-0010
Company Name
SPINEOLOGY INC.
Labeler DUNS
033014361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-16
Public Version
2
Public Version Date
2026-03-19
Public Version Status
Update
Public Device Record Key
d75a2eb1-7013-4097-935b-96070712f913

Device Description

8G x 19.3cm Pin Introducer Bevel

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
66937 Spinal intraoperative positioning/manipulation pin, single-use

Identifiers

Type ID
Primary M7403100010

Customer Contacts

Phone
651-256-8500

Device Sizes

Type Value Unit Text
Needle Gauge 8 Gauge
Length 19.3 Centimeter