FDA UDI In Commercial Distribution 🇺🇸 United States

SmartFrame OR

DI: 00850047354044 · Model: NGS-SFOR-BSF-01 · Clearpoint Neuro, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SmartFrame OR
Primary DI
00850047354044
Version / Model
NGS-SFOR-BSF-01
Catalog Number
NGS-SFOR-BSF-01
Company Name
Clearpoint Neuro, Inc.
Labeler DUNS
119078557
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-11
Public Version
1
Public Version Date
2024-03-19
Public Version Status
New
Public Device Record Key
9118dcd8-8d41-42bb-bcc9-0403e2eebbd7

Device Description

SmartFrame OR Bone Screw Fiducial Kit

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
Yes
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HAW Neurological Stereotaxic Instrument

GMDN Terms

Code Name
32568 Neurological stereotactic surgery system

Identifiers

Type ID
Primary 00850047354044

Customer Contacts

Phone
949-900-6833

Premarket Submissions

Submission Number Supplement Number
K233144 000