FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10885862553072 · Model: 01-007-30-0000 · Exactech, Inc.
Product Codes
7
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10885862553072
Version / Model
01-007-30-0000
Catalog Number
01-007-30-0000
Company Name
Exactech, Inc.
Labeler DUNS
157565946
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-28
Public Version
2
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
3bcf5940-2cf6-4b48-9b93-7a5eb6665ca8

Device Description

LINER DRIVER

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

Product Codes

Code Name
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
MEH Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
OQI Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented
LWJ Prosthesis, hip, semi-constrained, metal/polymer, uncemented
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
KWZ Prosthesis, hip, constrained, cemented or uncemented, metal/polymer

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 10885862553072

Premarket Submissions

Submission Number Supplement Number
K032964 000
K040601 000
K041906 000
K050398 000
K051556 000
K051682 000
K060107 000
K071676 000
K121392 000
K173583 000
K182502 000
K993082 000