The following data is part of a premarket notification filed by Encore Orthopedics, Inc. with the FDA for Foundation Porous Hip Stem.
Device ID | K973302 |
510k Number | K973302 |
Device Name: | FOUNDATION POROUS HIP STEM |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
Applicant | ENCORE ORTHOPEDICS, INC. 9800 METRIC BLVD. Austin, TX 78758 |
Contact | Debbie De Los Santos |
Correspondent | Debbie De Los Santos ENCORE ORTHOPEDICS, INC. 9800 METRIC BLVD. Austin, TX 78758 |
Product Code | LPH |
CFR Regulation Number | 888.3358 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-09-03 |
Decision Date | 1997-12-02 |
Summary: | summary |