FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00763000186258 · Model: FP9000X · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00763000186258
Version / Model
FP9000X
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-12
Public Version
3
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
c1141aad-4229-4175-b156-f0c7ab2ce296

Device Description

FIXATION BELT FP9000X EXTRA LARGE SCS PH

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
No

Product Codes

Code Name
LGW STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

GMDN Terms

Code Name
37685 Personal device holder, reusable

Identifiers

Type ID
Primary 00763000186258

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P840001 450