NEER-III OSTEOARTHRITIS GLENOID RESURFACE PROSTHE.— 510(k) K873620
Substantially Equivalent for Some IndicationsKirschner Medical Corp.
FDA 510(k) clearance K873620 for NEER-III OSTEOARTHRITIS GLENOID RESURFACE PROSTHE., Substantially Equivalent for Some Indications on 1987-10-15. Applicant: Kirschner Medical Corp..
Clearance details
- Applicant
- Kirschner Medical Corp.
- Product code
- Code KWT
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Timonium, MD, US
Adverse events under product code KWT
product code KWT- Injury
- 2,467
- Other
- 2
- Total
- 2,469
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.