FDA UDI In Commercial Distribution 🇺🇸 United States

Cervical Interbody Fusion Device

DI: B565CR1517101 · Model: CR1517-10 · Maxim Surgical
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cervical Interbody Fusion Device
Primary DI
B565CR1517101
Version / Model
CR1517-10
Catalog Number
CR1517-10
Company Name
Maxim Surgical
Labeler DUNS
012241561
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-21
Public Version
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
ec0761ea-3333-4983-9c6d-527490f9b8ac

Device Description

Cervical RASP 10 mm

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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary B565CR1517101

Customer Contacts

Phone
9723315860

Premarket Submissions

Submission Number Supplement Number
K123206 000

Device Sizes

Type Value Unit Text
Height 10 Millimeter