Identity
- Trade Name
- PHYSICA ZUK FDA UDI
- Generic Name
- Orthopaedic reamer guide FDA UDI
- Device Name
- Tibial EM Guide Cutting Block Connection FDA UDI
- Model / Reference
- Tibial EM Guide Cutting Block Connection FDA UDI
- Description
- Tibial EM Guide Cutting Block Connection FDA UDI
Identifiers
- Catalog Number
- 9061.20.063 FDA UDI
- Primary DI / UDI-DI
- 08033390128674 FDA UDI
- 510(k) Number
- K141934 FDA UDI
- FDA Product Code
- HRY FDA UDIJWH FDA UDI
- GMDN Term
- Orthopaedic reamer guide FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3530 FDA UDI888.3560 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: Orthopaedic reamer guide
Physica Zuk by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Orthopaedic reamer guide.
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- MAXIM EM TIBIAL GUIDE — Biomet Orthopedics, Inc. · Class I
Cleared under the same submission
K141934 also covers:
- MULTIGEN PLUS Knee — Limacorporate
- PHYSICA — 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 035d56a4-9080-437b-a259-9bf4a5ed3f63 35 fields · synced May 30, 2026