FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDOSKELETON® DPK

DI: 00191375010388 · Model: 750-1514-0 · TITAN SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON® DPK
Primary DI
00191375010388
Version / Model
750-1514-0
Catalog Number
750-1514-0
Company Name
TITAN SPINE, LLC
Labeler DUNS
623316978
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-15
Public Version
4
Public Version Date
2020-12-09
Public Version Status
Update
Public Device Record Key
744404d2-698c-4904-8853-9752c3905e82
Distribution End Date
2020-09-18

Device Description

Long Osteotome, 15in Length, 1/4in, Straight

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
35090 Surgical gouge

Identifiers

Type ID
Primary 00191375010388

Customer Contacts