The following data is part of a premarket notification filed by Biologically Oriented Prostheses with the FDA for Biopro Hemi-endo Modular Ceramic Head.
Device ID | K953045 |
510k Number | K953045 |
Device Name: | BIOPRO HEMI-ENDO MODULAR CERAMIC HEAD |
Classification | Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented |
Applicant | BIOLOGICALLY ORIENTED PROSTHESES 17 SEVENTEENTH ST. Port Huron, MI 48060 |
Contact | Marc F Malooley |
Correspondent | Marc F Malooley BIOLOGICALLY ORIENTED PROSTHESES 17 SEVENTEENTH ST. Port Huron, MI 48060 |
Product Code | LZO |
CFR Regulation Number | 888.3353 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-06-30 |
Decision Date | 1995-09-27 |