FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982304537 · Model: 04.172.630 · SYNTHES (U.S.A.) LP
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982304537
Version / Model
04.172.630
Catalog Number
04172630
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-13
Public Version
3
Public Version Date
2024-02-27
Public Version Status
Update
Public Device Record Key
9874b692-be2e-4f7d-ac84-9bf541caea85

Device Description

6.0MM TI BLUNTED POINT SCHANZ SCREW 30MM THRD/175MM

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
MR Conditional
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
OSN Software for diagnosis/treatment
HWC Screw, fixation, bone
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary 10886982304537

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K040701 000
K082650 000
K122455 000
K161417 000
K952296 000