FDA UDI In Commercial Distribution 🇺🇸 United States

A-Box®

DI: M711LAA0900 · Model: LAA-090 · Innovasis, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
A-Box®
Primary DI
M711LAA0900
Version / Model
LAA-090
Catalog Number
LAA-090
Company Name
Innovasis, Inc.
Labeler DUNS
156567492
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-05
Public Version
2
Public Version Date
2023-11-10
Public Version Status
Update
Public Device Record Key
1d8f2073-3cbc-47e6-a683-4104d4b918d3

Device Description

SST

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
Yes
Has Lot/Batch Number
No
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary M711LAA0900

Customer Contacts

Phone
801-261-2236

Premarket Submissions

Submission Number Supplement Number
K121581 000