FDA UDI Not in Commercial Distribution 🇺🇸 United States

Certex Spinal Fixation System

DI: M697X06706901 · Model: X067-0690 · Xtant Medical Holdings, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Certex Spinal Fixation System
Primary DI
M697X06706901
Version / Model
X067-0690
Company Name
Xtant Medical Holdings, Inc.
Labeler DUNS
081224143
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-11
Public Version
6
Public Version Date
2025-04-24
Public Version Status
Update
Public Device Record Key
1d3c8cc8-d4f3-416d-9b80-f881f964b8db
Distribution End Date
2024-12-16

Device Description

LAMINA PROBE

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
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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKG Posterior cervical screw system

GMDN Terms

Code Name
47862 Abdominal/ENT/orthopaedic surgical probe, reusable

Identifiers

Type ID
Direct Marking M697X06706900
Primary M697X06706901

Customer Contacts