FDA UDI In Commercial Distribution 🇺🇸 United States

OptiMesh Multiplanar Expandable Interbody Fusion System

DI: M7403150024 · Model: 35-01-31 · 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
M7403150024
Version / Model
35-01-31
Catalog Number
315-0024
Company Name
SPINEOLOGY INC.
Labeler DUNS
033014361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-17
Public Version
1
Public Version Date
2023-04-25
Public Version Status
New
Public Device Record Key
7300a7c7-a162-4383-a2fd-29df23e38ab5

Device Description

Manual Bent Tissue Extractor Brush

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
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary M7403150024

Customer Contacts

Phone
651-256-8500