FDA UDI In Commercial Distribution 🇺🇸 United States

Px™

DI: M711X210142500 · Model: X21014250 · Innovasis, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Px™
Primary DI
M711X210142500
Version / Model
X21014250
Catalog Number
X21014250
Company Name
Innovasis, Inc.
Labeler DUNS
156567492
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-16
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
7e069718-05a5-436f-b8f9-bbd7792f6fc5

Device Description

PEEK, Ta

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
Yes
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary M711X210142500

Customer Contacts

Phone
801-261-2236

Premarket Submissions

Submission Number Supplement Number
K150500 000

Device Sizes

Type Value Unit Text
Angle 0 degree
Length 25 Millimeter
Height 14 Millimeter
Width 10 Millimeter