FDA device listing
Appliance, Fixation, Spinal Intervertebral Body
FDA device listing 1304469719 · JAKUTEC Medizintechnik GmbH & Co. KG
Key facts
| Owner/operator | JAKUTEC Medizintechnik GmbH & Co. KG |
|---|---|
| Owner/operator number | 8010763 |
| Product codes | KWQ, NKB, PML |
| Device names | KWQ - Appliance, Fixation, Spinal Intervertebral Body, NKB - Thoracolumbosacral Pedicle Screw System, PML - Bone Cement, Posterior Screw Augmentation |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3027, 888.3060, 888.3070 |
| Review panels | Orthopedic |
| Registered establishments | JAKUTEC MEDIZINTECHNIK GMBH & Co. KG |
| Establishment registrations | 9612277 |
| FEI numbers | 3002807328 |
| Establishment operations | Contract Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database