icotec Interbody Cage System— 510(k) K172480
Substantially EquivalentIcotec AG
FDA 510(k) clearance K172480 for icotec Interbody Cage System, Substantially Equivalent on 2018-05-17. Applicant: Icotec AG. Device class: 2.
Clearance details
- Applicant
- Icotec AG
- Product code
- Code ODP
- Device class
- Class 2
- Regulation
- 21 CFR 888.3080
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- 9450 Altstaetten (Sg), CH
Recent devices under product code ODP
view allMore clearances from Icotec AG
view all- K252327 — CMORE® CT System; CMORE® CT System Navigated Instruments
- K242900 — VADER® Pedicle System and VADER®one Pedicle System
- K233215 — icotec Anterior Cervical Plate System
- K232792 — icotec Interbody Cage System (icotec Cervical Cage, icotec PLIF Lumbar Cage, icotec ETurn TLIF Lumbar Cage)
- K232790 — KONG®-TL VBR System and KONG® C VBR System
Adverse events under product code ODP
product code ODP- Injury
- 310
- Total
- 310
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.