FDA UDI In Commercial Distribution 🇺🇸 United States

Sochi

DI: 00843210173665 · Model: A16-18-1075 · Altus Spine, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sochi
Primary DI
00843210173665
Version / Model
A16-18-1075
Company Name
Altus Spine, LLC
Labeler DUNS
078331322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-03
Public Version
1
Public Version Date
2024-01-11
Public Version Status
New
Public Device Record Key
20f9d7f3-c26b-4047-a555-9423d949dd0d

Device Description

Pre-Curved Rod, 3.5mm x 75mm

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
KWP Appliance, Fixation, Spinal Interlaminal
NKG Posterior Cervical Screw System

GMDN Terms

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

Identifiers

Type ID
Primary 00843210173665

Customer Contacts

Phone
610-355-4156

Premarket Submissions

Submission Number Supplement Number
K210887 000