FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10885862295545 · Model: 521-50-07 · Exactech, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10885862295545
Version / Model
521-50-07
Catalog Number
521-50-07
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
1
Public Version Date
2022-08-05
Public Version Status
New
Public Device Record Key
4aa645de-5ad9-461b-8ad8-34ce7f0c3bc1

Device Description

TIBIAL TRAY TRACKER

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
OLO Orthopedic stereotaxic instrument
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
45200 Orthopaedic stereotactic surgery system

Identifiers

Type ID
Primary 10885862295545

Premarket Submissions

Submission Number Supplement Number
K100742 000
K152764 000
K193618 000