The following data is part of a premarket notification filed by Joint Medical Products Corp. with the FDA for Arthopor-acetabular Component.
| Device ID | K844050 |
| 510k Number | K844050 |
| Device Name: | ARTHOPOR-ACETABULAR COMPONENT |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented |
| Applicant | JOINT MEDICAL PRODUCTS CORP. 860 CANAL ST. Stamford, CT 06902 |
| Contact | Douglas G Noiles |
| Correspondent | Douglas G Noiles JOINT MEDICAL PRODUCTS CORP. 860 CANAL ST. Stamford, CT 06902 |
| Product Code | JDI |
| CFR Regulation Number | 888.3350 [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-10-17 |
| Decision Date | 1985-12-06 |