FDA UDI In Commercial Distribution 🇺🇸 United States

7.5 x 40mm CANN EXTENSION FASTENER

DI: 00810097801875 · Model: 101-75040 · Osteocentric Technologies, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
7.5 x 40mm CANN EXTENSION FASTENER
Primary DI
00810097801875
Version / Model
101-75040
Catalog Number
101-75040
Company Name
Osteocentric Technologies, Inc.
Labeler DUNS
089645059
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-13
Public Version
2
Public Version Date
2023-08-16
Public Version Status
Update
Public Device Record Key
19da5785-dd87-4d1c-9df6-25509f16519c

Device Description

7.5 x 40mm CANN EXTENSION FASTENER

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
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

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

Identifiers

Type ID
Primary 00810097801875

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K221332 000

Device Sizes

Type Value Unit Text
Outer Diameter 7.5 Millimeter
Length 40 Millimeter