FDA UDI In Commercial Distribution 🇺🇸 United States

Specify® SureScan®

DI: 00763000324230 · Model: 977C290 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Specify® SureScan®
Primary DI
00763000324230
Version / Model
977C290
Company Name
MEDTRONIC, INC.
Labeler DUNS
796986144
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-26
Public Version
1
Public Version Date
2022-03-07
Public Version Status
New
Public Device Record Key
d1fd2576-5381-4949-aa32-1a54277b8da3

Device Description

LEAD 977C290 SPECIFY SURESCAN 2X8 SRG

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LGW Stimulator, spinal-cord, totally implanted for pain relief
QRB Stimulator, spinal-cord, totally implanted for relief of pain due to diabetic neuropathy

GMDN Terms

Code Name
62423 Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection

Identifiers

Type ID
Primary 00763000324230

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P840001 497

Device Sizes

Type Value Unit Text
Length 90.0 Centimeter