FDA UDI Not in Commercial Distribution 🇺🇸 United States

PLEXUR P®

DI: 00643169218062 · Model: 60000525 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PLEXUR P®
Primary DI
00643169218062
Version / Model
60000525
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-20
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
64596ca0-29fc-4e60-99b5-81f5a074f79a
Distribution End Date
2017-02-09

Device Description

SHEET 60000525 PLEXUR P 100MMX25MMX4MM

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
Yes
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Safe
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
Yes

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MBP Filler, bone void, osteoinduction (w/o human growth factor)
MQV FILLER, BONE VOID, CALCIUM COMPOUND

GMDN Terms

Code Name
61403 Cadaveric-donor/synthetic polymer bone graft

Identifiers

Type ID
Primary 00643169218062

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K080511 000

Device Sizes

Type Value Unit Text
Height 4.0 Millimeter
Length 100.0 Millimeter
Width 25.0 Millimeter