FDA UDI In Commercial Distribution 🇺🇸 United States

Hive O-AL Interbody System

DI: 00817493027311 · Model: 02-A-1004-4015 · Nanohive Medical LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Hive O-AL Interbody System
Primary DI
00817493027311
Version / Model
02-A-1004-4015
Catalog Number
02-A-1004-4015
Company Name
Nanohive Medical LLC
Labeler DUNS
080469093
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-29
Public Version
2
Public Version Date
2025-07-14
Public Version Status
Update
Public Device Record Key
e22b7003-57f2-4d45-94ac-e0e26ec350f2

Device Description

38W x 34L, 15H, 12° - Jar Package Configuration

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00817493027311

Customer Contacts

Phone
844-943-5433

Premarket Submissions

Submission Number Supplement Number
K231241 000

Device Sizes

Type Value Unit Text
Width 38 Millimeter
Length 34 Millimeter
Angle 12 degree
Height 15 Millimeter