FDA UDI In Commercial Distribution 🇺🇸 United States

Cannulated Countersink, 2.2mm

DI: 00810054093374 · Model: SK22 · AVANTI ORTHOPAEDICS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cannulated Countersink, 2.2mm
Primary DI
00810054093374
Version / Model
SK22
Company Name
AVANTI ORTHOPAEDICS LLC
Labeler DUNS
043505370
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-02
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
e2a96390-ac67-4661-bbf5-fc5176457872

Device Description

Cannulated Countersink, 2.2mm

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
61689 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 00810054093374

Customer Contacts

Phone
610-316-7345

Premarket Submissions

Submission Number Supplement Number
K222967 000