HXW — Bender Class I
FDA Device Classification
Classification Details
- Product Code
- HXW
- Device Class
- Class I
- Regulation Number
- 888.4540
- Submission Type
- Review Panel
- OR
- Medical Specialty
- Orthopedic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K872949 | buckman co | ACROMED BONE PLATE BENDER | October 15, 1987 |
| K870668 | military engineering | DRIVER-BENDER-EXTRACTOR, BONE PIN | March 9, 1987 |
| K870084 | terray manufacturing | RD 140 SURGICAL BENDER | January 28, 1987 |