The following data is part of a premarket notification filed by Depuy Orthopaedics, Inc. with the FDA for Modification To Depuy Ceramic Femoral Head.
Device ID | K040644 |
510k Number | K040644 |
Device Name: | MODIFICATION TO DEPUY CERAMIC FEMORAL HEAD |
Classification | Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented |
Applicant | DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE Warsaw, IN 46581 -0988 |
Contact | Rebecca L Lennard |
Correspondent | Rebecca L Lennard DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE Warsaw, IN 46581 -0988 |
Product Code | LZO |
CFR Regulation Number | 888.3353 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-03-11 |
Decision Date | 2004-04-08 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10603295033646 | K040644 | 000 |