FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
Physica system
K Number: K213381
·
Decision Dec 17, 2021
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
64
Review Days
65
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Basic Information
- Device Name
- Physica system
- K Number
- K213381
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3560
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Lima Corporate S.P.A.
- Date Received
- October 13, 2021
- Decision Date
- December 17, 2021
- Product Code
- JWH
- Advisory Committee
- Orthopedic
- Review Advisory Committee
- OR
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | FDA class 2 | Orthopedic |
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Other Clearances by Lima Corporate S.P.A.
| K Number | Device Name | ||
|---|---|---|---|
| K252352 | SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral System | Jan 22, 2026 | Substantially Equivalent |
| K251718 | ArTT Augments and Buttresses and Bone Screws | Aug 29, 2025 | Substantially Equivalent |
| K243826 | SMR Reverse HP Shoulder System | Jul 3, 2025 | Substantially Equivalent |
| K250980 | Physica System (Physica CR Porous Femoral components) | May 22, 2025 | Substantially Equivalent |
| K243615 | Physica Porous Femoral Components | Dec 18, 2024 | Substantially Equivalent |
| K234011 | AMF TT Cones | Jan 18, 2024 | Substantially Equivalent |
| K233712 | PRIMA Humeral System; PRIMA TT Glenoid | Jan 11, 2024 | Substantially Equivalent |
| K231099 | SMR Hybrid Glenoid System | Dec 21, 2023 | Substantially Equivalent |
| K231925 | MINIMA S System | Jul 11, 2023 | Substantially Equivalent |
| K221758 | SMR Stemless Anatomic | Mar 17, 2023 | Substantially Equivalent |