AEQUOS
Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer
AAP IMPLANTATE AG
The following data is part of a premarket notification filed by Aap Implantate Ag with the FDA for Aequos.
Pre-market Notification Details
| Device ID | K033260 |
| 510k Number | K033260 |
| Device Name: | AEQUOS |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | AAP IMPLANTATE AG LORENZWEG 5 Berlin, DE 12099 |
| Contact | Marc Seegers |
| Correspondent | Marc Seegers AAP IMPLANTATE AG LORENZWEG 5 Berlin, DE 12099 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-10-09 |
| Decision Date | 2004-12-07 |
| Summary: | summary |
Trademark Results [AEQUOS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 AEQUOS 78226289 3013815 Dead/Cancelled |
aap Implantate AG 2003-03-17 |
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