TELIX K Interbody System— 510(k) K170890
Substantially EquivalentBiedermann Motech GmbH & Co. KG
FDA 510(k) clearance K170890 for TELIX K Interbody System, Substantially Equivalent on 2017-06-02. Applicant: Biedermann Motech GmbH & Co. KG.
Clearance details
- Applicant
- Biedermann Motech GmbH & Co. KG
- Product code
- Code MAX
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Villingen-Schwenningen, DE
Adverse events under product code MAX
product code MAX- Death
- 13
- Injury
- 1,305
- Malfunction
- 2,885
- Total
- 4,203
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.