The following data is part of a premarket notification filed by Mtd, Inc. with the FDA for Arthrostress.
| Device ID | K772321 |
| 510k Number | K772321 |
| Device Name: | ARTHROSTRESS |
| Classification | Table, Surgical With Orthopedic Accessories, Manual |
| Applicant | MTD, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JEB |
| CFR Regulation Number | 878.4950 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-12-19 |
| Decision Date | 1978-01-03 |