Identity
- Trade Name
- RESTORIS PST FDA UDI
- Generic Name
- Coated unicondylar knee tibia prosthesis FDA UDI
- Device Name
- Porous Tibial Baseplate FDA UDI
- Model / Reference
- 188613 FDA UDI
- Description
- Porous Tibial Baseplate FDA UDI
Identifiers
- Catalog Number
- 188613 FDA UDI
- Primary DI / UDI-DI
- 00848486016210 FDA UDI
- 510(k) Number
- K133811 FDA UDI
- FDA Product Code
- HRY FDA UDINJD FDA UDI
- GMDN Term
- Coated unicondylar knee tibia prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3530 FDA UDI888.3535 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Coated unicondylar knee tibia prosthesis
Restoris Pst by MAKO Surgical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Coated unicondylar knee tibia prosthesis.
- Unicondylar Sled Prosthesis — WALDEMAR LINK GmbH & Co. KG · Class II
- Unicondylar Sled Prosthesis — WALDEMAR LINK GmbH & Co. KG · Class II
- Unicondylar Sled Prosthesis — WALDEMAR LINK GmbH & Co. KG · Class II
- Symmetric Total Knee Tibial Tray — Signal Medical Corp. · Class II
- Uni Tibial Tray — Signal Medical Corp. · Class II
- Unicondylar Sled Prosthesis — WALDEMAR LINK GmbH & Co. KG · Class II
- Alliant Biotech — Medisurge · Class II
- Alliant Biotech — Medisurge · Class II
Cleared under the same submission
K133811 also covers:
- RESTORIS PST — MAKO Surgical Corp.
- RESTORIS PST — MAKO Surgical Corp.
- RESTORIS PST — MAKO Surgical Corp.
- RESTORIS PST — MAKO Surgical Corp.
- RESTORIS PST — MAKO Surgical Corp.
- RESTORIS PST — MAKO Surgical Corp.
- RESTORIS PST — MAKO Surgical Corp.
- RESTORIS PST — MAKO Surgical Corp.
- RESTORIS PST — MAKO Surgical Corp.
- RESTORIS PST — MAKO Surgical Corp.
- RESTORIS PST — MAKO Surgical Corp.
- RESTORIS PST — MAKO Surgical Corp.
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
- MAKO Surgical Corp.
Sources (1)
- FDA UDI c5b0faa9-dfd1-4323-8113-187a94d6e79f 36 fields · synced Jun 9, 2026