FDA UDI
In Commercial Distribution
🇺🇸 United States
iTotal Identity Posterior Stabilized Knee Replacement System
DI: M572RPS0102200131
·
Model: RPS010220013
·
Conformis, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- iTotal Identity Posterior Stabilized Knee Replacement System
- Primary DI
- M572RPS0102200131
- Version / Model
- RPS010220013
- Catalog Number
- RPS0102200
- Company Name
- Conformis, Inc.
- Labeler DUNS
- 808821883
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2020-07-06
- Public Version
- 1
- Public Version Date
- 2020-07-14
- Public Version Status
- New
- Public Device Record Key
- 732f6f59-0ea2-43be-a058-6408cc9a3ed5
Device Description
ITOTAL IDENTITY PS TIBIAL INSERT, NO TRIAL, IPOLY, 22MM
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
- Yes
- Has Lot/Batch Number
- No
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | Orthopedic | 888.3560 | 2 |
| OIY | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive | Orthopedic | 888.3560 | 2 |
| OOG | Knee Arthroplasty Implantation System | Orthopedic | 888.3560 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 46585 | Tibial insert | An implantable device designed to articulate the femoral and tibial components of a knee joint prosthesis during primary or revision bicondylar knee joint replacement. It is typically a one-piece contoured polyethylene (PE) insert, or a more complex device (e.g., a guide arm with a stem that is inserted into the tibial tray and a polymer glide) which will better reproduce the flexion of the knee joint due to its capacity for lateral rotation and anterior/posterior movement. This device is typically made of metal and/or a polymer. | Yes | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | M572RPS0102200131 | HIBCC |
Customer Contacts
- Phone
- 781-345-0001
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K201023 | 000 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Height | 22 | Millimeter |