The following data is part of a premarket notification filed by Aap Implantate Ag with the FDA for Aap Cannulated Screws.
| Device ID | K021233 |
| 510k Number | K021233 |
| Device Name: | AAP CANNULATED SCREWS |
| Classification | Screw, Fixation, Bone |
| Applicant | AAP IMPLANTATE AG LORENZWEG 5 Berlin, DE 12099 |
| Contact | Christian Abel |
| Correspondent | Christian Abel AAP IMPLANTATE AG LORENZWEG 5 Berlin, DE 12099 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-04-18 |
| Decision Date | 2002-12-09 |
| Summary: | summary |