FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDOSKELETON Posterior DPK

DI: M682110000150 · Model: 1100-0015 · TITAN SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON Posterior DPK
Primary DI
M682110000150
Version / Model
1100-0015
Catalog Number
1100-0015
Company Name
TITAN SPINE, LLC
Labeler DUNS
623316978
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-17
Public Version
5
Public Version Date
2020-12-09
Public Version Status
Update
Public Device Record Key
ea0b001b-6894-4539-884b-79d157e36f90
Distribution End Date
2020-09-21

Device Description

Angled Up, Bayonet, Ring Curette, 7mm

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary M682110000150

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Disc Prep Kit, Bayonet Ring Curette, Angled Up, 7mm
Length 15 Inch