The following data is part of a premarket notification filed by Allo Pro Corp. with the FDA for The Original Leinbach Platform Total Hip.
| Device ID | K820755 |
| 510k Number | K820755 |
| Device Name: | THE ORIGINAL LEINBACH PLATFORM TOTAL HIP |
| Classification | Prosthesis, Hip, Hemi-, Femoral, Metal |
| Applicant | ALLO PRO CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KWL |
| CFR Regulation Number | 888.3360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-03-19 |
| Decision Date | 1982-06-10 |