FDA UDI In Commercial Distribution 🇺🇸 United States

Responsive Orthopedics Total Knee Arthroplasty System

DI: 00841973106142 · Model: 90-SRK-201310 · RESPONSIVE ORTHOPEDICS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Responsive Orthopedics Total Knee Arthroplasty System
Primary DI
00841973106142
Version / Model
90-SRK-201310
Catalog Number
90-SRK-201310
Company Name
RESPONSIVE ORTHOPEDICS, LLC
Labeler DUNS
080074787
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-02
Public Version
5
Public Version Date
2019-04-23
Public Version Status
Update
Public Device Record Key
ad8b4301-ed9f-42bc-a58f-3fb0a3839a28

Device Description

EXTRACTOR 90-SRK-201310 TIBIAL TRAY

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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00841973106142