FDA device listing
Grappler Suture Anchor Extraosseous Crosswire System,Grappler Suture Anchor R3INFORCE System
FDA device listing 1504467427 · Paragon 28
Key facts
| Proprietary names | Grappler Suture Anchor Extraosseous Crosswire System,Grappler Suture Anchor R3INFORCE System |
|---|---|
| Owner/operator | Paragon 28 |
| Owner/operator number | 10033376 |
| Premarket submissions | K222091 |
| Product codes | MBI |
| Device names | MBI - Fastener, Fixation, Nondegradable, Soft Tissue |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3040 |
| Review panels | Orthopedic |
| Registered establishments | PARAGON 28 |
| Establishment registrations | 3008650117 |
| FEI numbers | 3008650117 |
| Establishment operations | Complaint File Establishment, Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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