The following data is part of a premarket notification filed by Stierlen-maquet Ag with the FDA for Extension Device 1416.
| Device ID | K873276 |
| 510k Number | K873276 |
| Device Name: | EXTENSION DEVICE 1416 |
| Classification | Table, Surgical With Orthopedic Accessories, Manual |
| Applicant | STIERLEN-MAQUET AG KEHLER STRASSE 31 7550 RASTATT West Germany, GR |
| Contact | Schnelle |
| Correspondent | Schnelle STIERLEN-MAQUET AG KEHLER STRASSE 31 7550 RASTATT West Germany, GR |
| Product Code | JEB |
| CFR Regulation Number | 878.4950 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-08-17 |
| Decision Date | 1987-09-17 |