TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER— 510(k) K032238
Substantially EquivalentNeurosel (Medical) Limited
FDA 510(k) clearance K032238 for TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER, Substantially Equivalent on 2003-09-09. Applicant: Neurosel (Medical) Limited.
Clearance details
- Applicant
- Neurosel (Medical) Limited
- Product code
- Code FZP
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Andover, Hampshire, GB
Adverse events under product code FZP
product code FZP- Death
- 11
- Injury
- 726
- Malfunction
- 10,830
- Other
- 1
- Total
- 11,568
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.