FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10705034779331 · Model: 406.101 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
10705034779331
Version / Model
406.101
Catalog Number
406101
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
6
Public Version Date
2025-07-02
Public Version Status
Update
Public Device Record Key
dda7db9f-2a62-4c26-b1cd-e67e21e5aff2
Distribution End Date
2019-02-14

Device Description

TI REPLACEMENT SETSCREW M5 STARDRIVE T15 CONICAL TIP

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
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

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Secondary H9814061010
Primary 10705034779331

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K023675 000