FDA UDI In Commercial Distribution 🇺🇸 United States

White Pearl Preferred Angle ACP

DI: B0622109110 · Model: 2100-9110 · Osseus Fusion Systems, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
White Pearl Preferred Angle ACP
Primary DI
B0622109110
Version / Model
2100-9110
Catalog Number
2100-9110
Company Name
Osseus Fusion Systems, LLC
Labeler DUNS
933442068
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-11
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
6abe8768-0f23-4bc3-8442-5729e98b4df5

Device Description

CERV SCREW, VARIABLE, SELF-DRILLING, 3.75x10mm, CORT/CANC, PREF ACP

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
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary B0622109110

Customer Contacts

Phone
888-330-5960

Premarket Submissions

Submission Number Supplement Number
K160522 000

Device Sizes

Type Value Unit Text
Length 10 Millimeter
Outer Diameter 3.75 Millimeter