SPAR-K Instruments (for use with Gemini SL Total Knee System)— 510(k) K191755
Substantially EquivalentWaldemar Link GmbH & Co. KG
FDA 510(k) clearance K191755 for SPAR-K Instruments (for use with Gemini SL Total Knee System), Substantially Equivalent on 2019-07-18. Applicant: Waldemar Link GmbH & Co. KG.
Clearance details
- Applicant
- Waldemar Link GmbH & Co. KG
- Product code
- Code JWH
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Norderstedt, DE
Adverse events under product code JWH
product code JWH- Death
- 26
- Injury
- 51,564
- Malfunction
- 9,725
- Other
- 9
- Total
- 61,324
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.