FDA UDI In Commercial Distribution 🇺🇸 United States

Headless Screw System

DI: M695401304330 · Model: 401-30433 · Tyber Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Headless Screw System
Primary DI
M695401304330
Version / Model
401-30433
Catalog Number
401-30433
Company Name
Tyber Medical, LLC
Labeler DUNS
010968002
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-13
Public Version
3
Public Version Date
2025-08-15
Public Version Status
Update
Public Device Record Key
8c0f9b76-6bee-4421-be34-59deee8b3f55

Device Description

Headless Ø3.0 x 33mm Full 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 M695401304330
Previous M695401304331Z

Premarket Submissions

Submission Number Supplement Number
K133842 000