The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Femoral Canal Sponge.
| Device ID | K831886 |
| 510k Number | K831886 |
| Device Name: | FEMORAL CANAL SPONGE |
| Classification | Gauze / Sponge,nonresorbable For External Use |
| Applicant | ZIMMER, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | NAB |
| CFR Regulation Number | 878.4014 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-06-13 |
| Decision Date | 1983-09-12 |