Identity
- Trade Name
- PHYSICA PS FDA UDI
- Generic Name
- Knee femur prosthesis trial, reusable FDA UDI
- Device Name
- #1-Right-Trial Femoral Component FDA UDI
- Model / Reference
- Trial Femoral Component FDA UDI
- Description
- #1-Right-Trial Femoral Component FDA UDI
Identifiers
- Catalog Number
- 9065.15.110 FDA UDI
- Primary DI / UDI-DI
- 08033390096379 FDA UDI
- 510(k) Number
- K152008 FDA UDI
- FDA Product Code
- JWH FDA UDI
- GMDN Term
- Knee femur prosthesis trial, reusable 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
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Knee femur prosthesis trial, reusable
Physica Ps by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Knee femur prosthesis trial, reusable.
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- Natural-Knee® — Zimmer, Inc. · Class II
- NexGen® — Zimmer, Inc. · Class II
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- Persona® — Zimmer, Inc. · Class II
Cleared under the same submission
K152008 also covers:
- PHYSICA Instrument Set — Limacorporate
- PHYSICA Instrument Set — Limacorporate
- PHYSICA Instrument Set — Limacorporate
- PHYSICA Instrument Set — Limacorporate
- PHYSICA Instrument Set — Limacorporate
- PHYSICA Instrument Set — Limacorporate
- PHYSICA Instrument Set — Limacorporate
- PHYSICA Instrument Set — Limacorporate
- PHYSICA Instrument Set — Limacorporate
- PHYSICA Instrument Set — Limacorporate
- PHYSICA Instrument Set — Limacorporate
- PHYSICA Instrument Set — Limacorporate
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Limacorporate
Sources (1)
- FDA UDI c3190abd-5408-4183-b6f6-d0e22720bfa8 36 fields · synced May 31, 2026