FDA UDI Not in Commercial Distribution 🇺🇸 United States

PERIMETER™ System

DI: 00643169167773 · Model: X1111489 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PERIMETER™ System
Primary DI
00643169167773
Version / Model
X1111489
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
2015-07-01
Public Version
5
Public Version Date
2022-05-09
Public Version Status
Update
Public Device Record Key
8d3a1af8-810c-4cd6-8e52-dc4e7e2d9c75
Distribution End Date
2022-05-03

Device Description

SPACER X1111489 PERIMETER LG 8DEG 9MM

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00643169167773

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K090353 000

Device Sizes

Type Value Unit Text
Device Size Text, specify LG
Width 30.0 Millimeter
Length 24.0 Millimeter
Height 9.0 Millimeter