The following data is part of a premarket notification filed by Implex Corp. with the FDA for Implex A-230 Porous Acetabular Cup Syst.cementless.
| Device ID | K932923 |
| 510k Number | K932923 |
| Device Name: | IMPLEX A-230 POROUS ACETABULAR CUP SYST.CEMENTLESS |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
| Applicant | IMPLEX CORP. 80 COMMERCE DR. Allendale, NJ 07401 -1600 |
| Contact | James E Malayter |
| Correspondent | James E Malayter IMPLEX CORP. 80 COMMERCE DR. Allendale, NJ 07401 -1600 |
| Product Code | LPH |
| CFR Regulation Number | 888.3358 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-15 |
| Decision Date | 1994-05-03 |