The following data is part of a premarket notification filed by Kinamed, Inc. with the FDA for Kinamed 26mm Bioceran-z Total Hip Femoral Ball.
Device ID | K920219 |
510k Number | K920219 |
Device Name: | KINAMED 26MM BIOCERAN-Z TOTAL HIP FEMORAL BALL |
Classification | Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented |
Applicant | KINAMED, INC. 2000 M ST. N.W SUITE 700 Washington, DC 20036 |
Contact | Daniel J Manelli |
Correspondent | Daniel J Manelli KINAMED, INC. 2000 M ST. N.W SUITE 700 Washington, DC 20036 |
Product Code | LZO |
CFR Regulation Number | 888.3353 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-01-16 |
Decision Date | 1992-10-30 |