CHARNLEY FEMUR DRILL #1 AND #2— 510(k) K760977
Substantially EquivalentCodman & Shurtleff, Inc.
FDA 510(k) clearance K760977 for CHARNLEY FEMUR DRILL #1 AND #2, Substantially Equivalent on 1976-11-16. Applicant: Codman & Shurtleff, Inc.. Device class: 1.
Clearance details
- Applicant
- Codman & Shurtleff, Inc.
- Product code
- Code HWE
- Device class
- Class 1
- Regulation
- 21 CFR 878.4820
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Adverse events under product code HWE
product code HWE- Death
- 4
- Injury
- 448
- Malfunction
- 19,856
- Other
- 2
- Total
- 20,310
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.