K830356 is an FDA 510(k) clearance for the TITANIUM M.E. MULLER TYPE TOTAL HIP. This device is classified as a Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented (Class II - Special Controls, product code JDI).
Submitted by Boehringer Mannheim Corp. (Mchenry, US). The FDA issued a Cleared decision on March 9, 1983, 34 days after receiving the submission on February 3, 1983.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3350.
| 510(k) Number | K830356 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 03, 1983 |
| Decision Date | March 09, 1983 |
| Days to Decision | 34 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | — |
| Product Code | JDI — Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3350 |