The following data is part of a premarket notification filed by Dow Corning Wright with the FDA for Whiteside Ortholoc Calcar Replacement Hip Stem Pro.
| Device ID | K874740 |
| 510k Number | K874740 |
| Device Name: | WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO |
| Classification | Prosthesis, Hip, Femoral Component, Cemented, Metal |
| Applicant | DOW CORNING WRIGHT P.O. BOX 100 Arlington, TN 38002 |
| Contact | Lipscomb, Phd |
| Correspondent | Lipscomb, Phd DOW CORNING WRIGHT P.O. BOX 100 Arlington, TN 38002 |
| Product Code | JDG |
| CFR Regulation Number | 888.3360 [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-11-18 |
| Decision Date | 1987-12-18 |