FDA UDI Not in Commercial Distribution 🇺🇸 United States

PERPOS PLS SYSTEM, Dual Implant

DI: 81195401005824 · Model: 9045-02 · INTERVENTIONAL SPINE, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PERPOS PLS SYSTEM, Dual Implant
Primary DI
81195401005824
Version / Model
9045-02
Catalog Number
9045-02
Company Name
INTERVENTIONAL SPINE, INC
Labeler DUNS
017663522
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
a2b62f07-ebee-42b7-b4aa-95dab33ec531
Distribution End Date
2016-12-23

Device Description

2 Bone-Lok PLS Implant

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Safe
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
MRW System, Facet Screw Spinal Device

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 81195401005824

Customer Contacts

Phone
800-497-0484