The following data is part of a premarket notification filed by Intermedics Orthopedics with the FDA for Select Shoulder Concentric Humeral Head Components.
Device ID | K962224 |
510k Number | K962224 |
Device Name: | SELECT SHOULDER CONCENTRIC HUMERAL HEAD COMPONENTS |
Classification | Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented |
Applicant | INTERMEDICS ORTHOPEDICS 9900 SPECTRUM DR. Austin, TX 78717 |
Contact | Mitchell A Dhority |
Correspondent | Mitchell A Dhority INTERMEDICS ORTHOPEDICS 9900 SPECTRUM DR. Austin, TX 78717 |
Product Code | KWS |
Subsequent Product Code | HSD |
Subsequent Product Code | KWT |
CFR Regulation Number | 888.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-06-10 |
Decision Date | 1996-08-28 |
Summary: | summary |