The following data is part of a premarket notification filed by Ebi, L.p. with the FDA for Ebi Distal Radius Plating System.
Device ID | K040908 |
510k Number | K040908 |
Device Name: | EBI DISTAL RADIUS PLATING SYSTEM |
Classification | Plate, Fixation, Bone |
Applicant | EBI, L.P. 399 JEFFERSON ROAD Parsippany, NJ 07054 |
Contact | Frederic Testa |
Correspondent | Frederic Testa EBI, L.P. 399 JEFFERSON ROAD Parsippany, NJ 07054 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-04-07 |
Decision Date | 2004-06-25 |
Summary: | summary |