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Modular Construct Frame External Fixa
FDA 510(k)Class II (US FDA 510(k))
510(k) K840856
Identifiers
- 510(k) Number
- K840856 FDA 510(k)
- FDA Product Code
- JEC FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 888.3040 FDA 510(k)
- Regulation Number
- 888.3040 FDA 510(k)
- Advisory Committee
- Orthopedic FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Modular Construct Frame External Fixa by Precision Medical Devices, Inc. — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K840856 | Class II | Active |
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Manufacturer
- Manufacturer
- Precision Medical Devices, Inc.
Sources (1)
- FDA 510(k) K840856 24 fields · synced Jun 18, 2026