The following data is part of a premarket notification filed by Acumed Llc with the FDA for Acumed Congruent Bone Plate System.
Device ID | K063460 |
510k Number | K063460 |
Device Name: | ACUMED CONGRUENT BONE PLATE SYSTEM |
Classification | Plate, Fixation, Bone |
Applicant | ACUMED LLC 5885 NW CORNELIUS PASS RD. Hillsboro, OR 97124 -9432 |
Contact | Ed Boehmer |
Correspondent | Ed Boehmer ACUMED LLC 5885 NW CORNELIUS PASS RD. Hillsboro, OR 97124 -9432 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-11-15 |
Decision Date | 2006-12-07 |
Summary: | summary |