The following data is part of a premarket notification filed by Exactech, Inc. with the FDA for Exactech Novation Crown Cup And Liners.
Device ID | K070479 |
510k Number | K070479 |
Device Name: | EXACTECH NOVATION CROWN CUP AND LINERS |
Classification | Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented |
Applicant | EXACTECH, INC. 2320 N.W. 66TH CT. Gainesville, FL 32653 |
Contact | Maritza Elias |
Correspondent | Maritza Elias EXACTECH, INC. 2320 N.W. 66TH CT. Gainesville, FL 32653 |
Product Code | LZO |
Subsequent Product Code | JDI |
Subsequent Product Code | LPH |
Subsequent Product Code | LWJ |
Subsequent Product Code | MEH |
CFR Regulation Number | 888.3353 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-02-20 |
Decision Date | 2007-03-15 |
Summary: | summary |