FDA UDI In Commercial Distribution 🇺🇸 United States

Kinectiv®

DI: 00889024509580 · Model: 00-7848-041-01 · Zimmer, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kinectiv®
Primary DI
00889024509580
Version / Model
00-7848-041-01
Catalog Number
00-7848-041-01
Company Name
Zimmer, Inc.
Labeler DUNS
056038268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-14
Public Version
2
Public Version Date
2019-08-07
Public Version Status
Update
Public Device Record Key
5c219005-cb0f-460e-80c0-63bac26d2572

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
MR Conditional
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
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
LWJ Prosthesis, hip, semi-constrained, metal/polymer, uncemented
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

GMDN Terms

Code Name
55833 Press-fit hip femur prosthesis, modular

Identifiers

Type ID
Primary 00889024509580

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K071856 000
K182678 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 12/14 Neck Taper