TDM Lumbar Interbody Fusion Cage System— 510(k) K221844
Substantially EquivalentTdm Co., Ltd.
FDA 510(k) clearance K221844 for TDM Lumbar Interbody Fusion Cage System, Substantially Equivalent on 2022-08-17. Applicant: Tdm Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Tdm Co., Ltd.
- Product code
- Code MAX
- Device class
- Class 2
- Regulation
- 21 CFR 888.3080
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Gwangju, KR
Recent devices under product code MAX
view allMore clearances from Tdm Co., Ltd.
view all- K241128 — TDM Plate and Screw System
- K230071 — Femur Reconstruction Interlocking Nail System, Femur Retrograde Interlocking Nail System, Humerus Interlocking Nail System, Tibia Interlocking Nail System, Compression Hip Nail System
- K240423 — TDM Anterior Cervical Plate System
- K232115 — TDM Large Bone Plate and Screw System
- K231860 — TDM Screw System
Adverse events under product code MAX
product code MAX- Death
- 13
- Injury
- 1,305
- Malfunction
- 2,885
- Total
- 4,203
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.