DWH — Blade, Saw, Surgical, Cardiovascular Class I
FDA product code DWH covers "Blade, Saw, Surgical, Cardiovascular", a Class I medical device regulated under 21 CFR 878.4820. Submissions are reviewed by the General, Plastic Surgery panel. At least 4 recent 510(k) clearances have been granted under this product code.
Classification Details
- Product Code
- DWH
- Device Class
- Class I
- Regulation Number
- 878.4820
- Submission Type
- Review Panel
- SU
- Medical Specialty
- General, Plastic Surgery
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K904352 | codman and shurtleff | CODMAN COLLINS RADIOPARENT STERNAL BLADES | November 21, 1990 |
| K862474 | hall surgical, division of zimmer | HALL STERNUM SAW | July 17, 1986 |
| K850483 | micro-aire surgical instruments | MICRO-AIRE STERNUM SAW REPLACEMENT BLADES | March 1, 1985 |
| K830189 | temp medical products | CARDIOVASCULAR SAW BLADES | March 24, 1983 |