K800144 is an FDA 510(k) clearance for the FEMORAL CEMENT RESTRICTOR. This device is classified as a Nail, Fixation, Bone (Class II - Special Controls, product code JDS).
Submitted by Biomet, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 19, 1980, 29 days after receiving the submission on January 21, 1980.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3030.
| 510(k) Number | K800144 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 21, 1980 |
| Decision Date | February 19, 1980 |
| Days to Decision | 29 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | — |
| Product Code | JDS — Nail, Fixation, Bone |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3030 |