FDA Product Code
FDA Product Code HWR — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Orthopedic
- 21 CFR Citation
- 888.4540
510(k) Clearances — 4 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K915776 | KNEE PROSTHESIS DRIVER | Kim-Med, Inc. | 1992-06-11 | Traditional | PDF ↗ |
| K875054 | ACROMED ADS BONE NAIL DRIVER | Buckman Co., Inc. | 1988-01-28 | Traditional | PDF ↗ |
| K870848 | SCHULTZ METACARPAL COMPONENT DRIVER | Warsaw Orthopedic, Inc. | 1987-03-13 | Traditional | PDF ↗ |
| K870847 | SCHULTZ PHALANGEAL COMPONENT DRIVER | Warsaw Orthopedic, Inc. | 1987-03-13 | Traditional | PDF ↗ |
Product code HWR · Class I · Orthopedic. Data: openFDA.