V-LOC 180 ABSORBABLE WOUND CLOSURE DEVICE— 510(k) K082662
Substantially EquivalentSurgical Devices, Tyco Healthcare Group LP
FDA 510(k) clearance K082662 for V-LOC 180 ABSORBABLE WOUND CLOSURE DEVICE, Substantially Equivalent on 2009-03-26. Applicant: Surgical Devices, Tyco Healthcare Group LP.
Clearance details
- Applicant
- Surgical Devices, Tyco Healthcare Group LP
- Product code
- Code GAM
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- North Haven, CT, US
Adverse events under product code GAM
product code GAM- Death
- 45
- Injury
- 5,711
- Malfunction
- 30,744
- Other
- 4
- Total
- 36,504
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.