FDA UDI In Commercial Distribution 🇺🇸 United States

Orbitum Staple System

DI: B565FO20212001 · Model: Rev A · CPM MEDICAL CONSULTANTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Orbitum Staple System
Primary DI
B565FO20212001
Version / Model
Rev A
Catalog Number
FO-2021-20
Company Name
CPM MEDICAL CONSULTANTS, LLC
Labeler DUNS
017138000
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-10
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
701ffb7e-eb32-49d9-a7fe-abf8fa80e3d2

Device Description

20MM Planer

Device Characteristics

Single Use
No
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
JDR Staple, Fixation, Bone

GMDN Terms

Code Name
35685 Orthopaedic bone wire

Identifiers

Type ID
Primary B565FO20212001

Premarket Submissions

Submission Number Supplement Number
K173693 000