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icotec Interbody Cage System (icotec Cervical Cage +2 more)
FDA 510(k)Class II (US FDA 510(k))
510(k) K232792
by icotec AG
Identifiers
- 510(k) Number
- K232792 FDA 510(k)
- FDA Product Code
- MAX FDA 510(k)
- Models / Variants
- icotec Cervical Cage FDA 510(k)icotec PLIF Lumbar Cage FDA 510(k)icotec ETurn™ TLIF Lumbar Cage FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 888.3080 FDA 510(k)
- Regulation Number
- 888.3080 FDA 510(k)
- Advisory Committee
- Orthopedic FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
icotec Interbody Cage System (icotec Cervical Cage +2 more) by icotec AG — Class II — FDA_510K — listed in FDA 510(k) — 3 models — 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 | K232792 | Class II | Active |
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Manufacturer
- Manufacturer
- icotec AG
Sources (1)
- FDA 510(k) K232792 24 fields · synced Jun 18, 2026