The following data is part of a premarket notification filed by Intermedics Orthopedics with the FDA for Rim Flare Acetabular Component.
Device ID | K955033 |
510k Number | K955033 |
Device Name: | RIM FLARE ACETABULAR COMPONENT |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
Applicant | INTERMEDICS ORTHOPEDICS 9900 SPECTRUM DR. Austin, TX 78717 |
Contact | Jacquelyn Hughes |
Correspondent | Jacquelyn Hughes INTERMEDICS ORTHOPEDICS 9900 SPECTRUM DR. Austin, TX 78717 |
Product Code | LPH |
CFR Regulation Number | 888.3358 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-11-02 |
Decision Date | 1996-01-31 |