The following data is part of a premarket notification filed by Plus Orthopedics with the FDA for Modular Plus Hip Stem.
Device ID | K032709 |
510k Number | K032709 |
Device Name: | MODULAR PLUS HIP STEM |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Uncemented |
Applicant | PLUS ORTHOPEDICS 1001 OAKWOOD BLVD. Round Rock, TX 78681 -2700 |
Contact | J.d. Webb |
Correspondent | J.d. Webb PLUS ORTHOPEDICS 1001 OAKWOOD BLVD. Round Rock, TX 78681 -2700 |
Product Code | LWJ |
CFR Regulation Number | 888.3360 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-09-02 |
Decision Date | 2003-09-23 |
Summary: | summary |