The following data is part of a premarket notification filed by Depuy Orthopaedics, Inc. with the FDA for Depuy Global Ap Cta Humeral Head.
| Device ID | K082715 |
| 510k Number | K082715 |
| Device Name: | DEPUY GLOBAL AP CTA HUMERAL HEAD |
| Classification | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented |
| Applicant | DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE Warsaw, IN 46581 -0988 |
| Contact | Rhonda Myer |
| Correspondent | Rhonda Myer DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE Warsaw, IN 46581 -0988 |
| Product Code | HSD |
| CFR Regulation Number | 888.3690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-09-17 |
| Decision Date | 2008-12-18 |
| Summary: | summary |