Offset Tibial Tray
FDA 510(k) K010212 · Biomet, Inc.
510(k) numberK010212
Submission
- Device name
- Offset Tibial Tray
- Applicant
- Biomet, Inc.
Warsaw, IN, US - Received
- January 23, 2001
- Decision date
- February 14, 2001
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MBV – Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uhmwpe, Pegged, Cemented, Polymer/Metal/Polymer
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3560
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code MBV
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K884824 | Tricon-M Total Knee SystemMBV · Traditional | Richards Medical Co., Inc. | 11/21/1989SN |
| K873429 | Freeman-Samuelson Mark II Press-Fit Total KneeMBV · Traditional | Protek, Inc. | 10/28/1987SE |
| K853730 | Freeman-Samuelson Mark II Press-Fit Total Knee RepMBV · Traditional | Protek, Inc. | 02/18/1986SE |
| K833200 | Tricon M Total Knee SystemMBV · Traditional | Richards Medical Co., Inc. | 11/29/1983SE |
| K831441 | Porocoat Freeman/Samuelson Total KneeMBV · Traditional | Depuy, Inc. | 09/01/1983SE |
| K832302 | Mark I Total Knee Sys. ArthroplastyMBV · Traditional | Advanced Biosearch Assn. | 08/16/1983SE |
| K830726 | Mark I & II Total Knee Replace. SysMBV · Traditional | Advanced Biosearch Assn. | 06/22/1983SE |
| K823837 | RMC Total Knee SystemMBV · Traditional | Richard'S Medical Equip., Inc. | 03/29/1983SE |
| K830408 | Freeman/Samuelson Total KneeMBV · Traditional | Depuy, Inc. | 02/24/1983SE |
| K822583 | Total Knee SystemMBV · Traditional | Richard'S Medical Equip., Inc. | 10/04/1982SE |
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| 510(k) | Device | Decision |
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| K241014 | Biomet Kirschner Wires (K-Wires)HTY · Traditional | 05/22/2024SE |
| K222760 | StageOne Select Hip Cement Spacer MoldsMBB · Traditional | 12/28/2022SE |
| K221968 | StageOne Shoulder Cement Spacer MoldsMBB · Traditional | 09/15/2022SE |
| K213287 | StageOne Knee Cement Spacer MoldsMBB · Traditional | 09/02/2022SE |
| K212431 | Biomet Answer/Impact/Integral Distal Centralizer/Centering SleeveJDG · Traditional | 02/07/2022SE |
| K212435 | Comprehensive Humeral Fracture Positioning SleevesKWS · Traditional | 12/10/2021SE |
| K210192 | A.L.P.S. Clavicle Plating SystemHRS · Special | 02/19/2021SE |
| K193214 | WasherLoc and No-Profile Screw and Washer Systems, Biomet Cannulated Screw System…MBI · Traditional | 11/10/2020SE |
Questions and answers
When was Offset Tibial Tray cleared by the FDA?
Offset Tibial Tray (K010212) received a 510(k) decision of Substantially Equivalent on February 14, 2001, 22 days after the submission was received.
What is the product code of K010212?
The FDA product code is MBV – Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uhmwpe, Pegged, Cemented, Polymer/Metal/Polymer, a Class II (moderate risk) device regulated under 21 CFR 888.3560.