The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Herbert Bone Screw.
| Device ID | K792022 |
| 510k Number | K792022 |
| Device Name: | HERBERT BONE SCREW |
| Classification | Screw, Fixation, Bone |
| Applicant | ZIMMER, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-10-09 |
| Decision Date | 1979-10-26 |