FDA UDI In Commercial Distribution 🇺🇸 United States

Headless Screw System

DI: M695401203200 · Model: 401-20320 · Tyber Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Headless Screw System
Primary DI
M695401203200
Version / Model
401-20320
Catalog Number
401-20320
Company Name
Tyber Medical, LLC
Labeler DUNS
010968002
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-23
Public Version
3
Public Version Date
2025-08-15
Public Version Status
Update
Public Device Record Key
6c1b3937-510d-46a8-8449-baada036edd0

Device Description

Headless Ø2.0 x 20mm Long Thread Ti (Torx)

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary M695401203200
Previous M695401203201T

Premarket Submissions

Submission Number Supplement Number
K133842 000