The following data is part of a premarket notification filed by Howmedica Corp. with the FDA for Asnis Guided Screw Systems.
| Device ID | K801969 |
| 510k Number | K801969 |
| Device Name: | ASNIS GUIDED SCREW SYSTEMS |
| Classification | Specula, Ophthalmic |
| Applicant | HOWMEDICA CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HNC |
| CFR Regulation Number | 886.4350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-08-19 |
| Decision Date | 1980-08-27 |