K790331 is an FDA 510(k) clearance for the ZIMMER SURGICAL INSTRUMENT LUBRICANT..
Submitted by Zimmer, Inc. (Mchenry, US). The FDA issued a Cleared decision on April 3, 1979, 46 days after receiving the submission on February 16, 1979.
This device falls under the General & Plastic Surgery FDA review panel.
| 510(k) Number | K790331 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 16, 1979 |
| Decision Date | April 03, 1979 |
| Days to Decision | 46 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | — |
| Device Class | — |