FDA UDI In Commercial Distribution 🇺🇸 United States

Trestle Luxe

DI: 00844856067288 · Model: 71240-10 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trestle Luxe
Primary DI
00844856067288
Version / Model
71240-10
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-01
Public Version
7
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
586da1a3-6a82-45fd-a2c0-41bc3b5b1e02

Device Description

4.0mm Variable Angle, Self-Drilling Hexalobe Screw, 10mm

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
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 00844856067288

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K102820 000

Device Sizes

Type Value Unit Text
Length 10 Millimeter