ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTES— 510(k) K954052
Substantially Equivalent for Some IndicationsT. Korossurgical Instruments Corp.
FDA 510(k) clearance K954052 for ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTES, Substantially Equivalent for Some Indications on 1995-11-06. Applicant: T. Korossurgical Instruments Corp..
Clearance details
- Applicant
- T. Korossurgical Instruments Corp.
- Product code
- Code HRX
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Moorepark, CA, US
Adverse events under product code HRX
product code HRX- Injury
- 623
- Malfunction
- 11,257
- Total
- 11,880
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.