The following data is part of a premarket notification filed by Nexa Orthopedics, Inc. with the FDA for Nexa Compression Screw.
Device ID | K060071 |
510k Number | K060071 |
Device Name: | NEXA COMPRESSION SCREW |
Classification | Screw, Fixation, Bone |
Applicant | NEXA ORTHOPEDICS, INC. 10675 SORRENTO VALLEY ROAD SUITE 100 San Diego, CA 92121 |
Contact | Louise M Focht |
Correspondent | Louise M Focht NEXA ORTHOPEDICS, INC. 10675 SORRENTO VALLEY ROAD SUITE 100 San Diego, CA 92121 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-01-09 |
Decision Date | 2006-01-26 |
Summary: | summary |