WMT COMPOSITE DBM— 510(k) K083270
Substantially EquivalentWrightmedicaltechnologyinc
FDA 510(k) clearance K083270 for WMT COMPOSITE DBM, Substantially Equivalent on 2009-08-27. Applicant: Wrightmedicaltechnologyinc. Device class: 2.
Clearance details
- Applicant
- Wrightmedicaltechnologyinc
- Product code
- Code MQV
- Device class
- Class 2
- Regulation
- 21 CFR 888.3045
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Arlington, TN, US
Recent devices under product code MQV
view allMore clearances from Wrightmedicaltechnologyinc
view allAdverse events under product code MQV
product code MQV- Death
- 6
- Injury
- 435
- Total
- 441
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 →
Recalls naming K083270
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K083270.
Data sourced from openFDA. This site is unofficial and independent of the FDA.