The following data is part of a premarket notification filed by Encore Medical, L.p with the FDA for Altivate Anatomic Shoulder System.
Device ID | K162024 |
510k Number | K162024 |
Device Name: | AltiVate Anatomic Shoulder System |
Classification | Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented |
Applicant | ENCORE MEDICAL, L.P 9800 METRIC BLVD. Austin, TX 78758 |
Contact | Desiree Wells |
Correspondent | Desiree Wells ENCORE MEDICAL, L.P 9800 METRIC BLVD. Austin, TX 78758 |
Product Code | KWS |
Subsequent Product Code | HSD |
Subsequent Product Code | PAO |
CFR Regulation Number | 888.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-07-22 |
Decision Date | 2016-11-21 |
Summary: | summary |