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iTotal Identity Posterior Stabilized Knee Replacement System
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- iTotal Identity Posterior Stabilized Knee Replacement System FDA UDI
- Generic Name
- Tibial insert FDA UDI
- Device Name
- ITOTAL IDENTITY PS TIBIAL INSERT + TRIAL, IPOLY, 8MM FDA UDI
- Model / Reference
- RPS010080003 FDA UDI
- Description
- ITOTAL IDENTITY PS TIBIAL INSERT + TRIAL, IPOLY, 8MM FDA UDI
Identifiers
- Catalog Number
- RPS-010-0800 FDA UDI
- Primary DI / UDI-DI
- M572RPS0100800031 FDA UDI
- 510(k) Number
- K201023 FDA UDI
- FDA Product Code
- JWH FDA UDIOIY FDA UDIOOG FDA UDI
- GMDN Term
- Tibial insert FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3560 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Height — 8 Millimeter FDA UDI
Category: Tibial insert
iTotal Identity Posterior Stabilized Knee Replacement System by Conformis, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Tibial insert.
- DJO SURGICAL — ENCORE MEDICAL, L.P. · Class II
- P.F.C. SIGMA — DEPUY (IRELAND) · Class II
- Truliant, Activit-E — Exactech, Inc. · Class II
- Maxim Knee System — Biomet Orthopedics, Inc. · Class II
- Scorpio — Howmedica Osteonics Corp. · Class II
- TriVerse Meniscal Insert PS+ — SIGNATURE ORTHOPAEDICS PTY LTD · Class II
- Scorpio — Howmedica Osteonics Corp. · Class II
- World Knee System — SIGNATURE ORTHOPAEDICS PTY LTD · Class II
Cleared under the same submission
K201023 also covers:
- iTotal Identity PS — Conformis, Inc.
- iTotal Identity Posterior Stabilized Knee Replacement System — Conformis, Inc.
- iTotal Identity Posterior Stabilized Knee Replacement System — Conformis, Inc.
- iTotal Identity Posterior Stabilized Knee Replacement System — Conformis, Inc.
- iTotal Identity Posterior Stabilized Knee Replacement System — Conformis, Inc.
- iTotal Identity Posterior Stabilized Knee Replacement System — Conformis, Inc.
- iTotal Identity Posterior Stabilized Knee Replacement System — Conformis, Inc.
- iTotal Identity Posterior Stabilized Knee Replacement System — Conformis, Inc.
- iTotal Identity Posterior Stabilized Knee Replacement System — Conformis, Inc.
- iTotal Identity Posterior Stabilized Knee Replacement System — Conformis, Inc.
- iTotal Identity Posterior Stabilized Knee Replacement System — Conformis, Inc.
- iTotal Identity Posterior Stabilized Knee Replacement System — Conformis, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Conformis, Inc.
Sources (1)
- FDA UDI 8458b5e5-8265-4c26-8797-3a2e41fde9bb 37 fields · synced May 30, 2026