The following data is part of a premarket notification filed by Mako Surgical Corporation with the FDA for Mako Modular Knee Compartmental Implant System.
Device ID | K082172 |
510k Number | K082172 |
Device Name: | MAKO MODULAR KNEE COMPARTMENTAL IMPLANT SYSTEM |
Classification | Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer |
Applicant | MAKO SURGICAL CORPORATION 2555 DAVIE ROAD Fort Lauderdale, FL 33317 |
Contact | William F Tapia |
Correspondent | William F Tapia MAKO SURGICAL CORPORATION 2555 DAVIE ROAD Fort Lauderdale, FL 33317 |
Product Code | HSX |
Subsequent Product Code | HRY |
Subsequent Product Code | KRR |
Subsequent Product Code | NPJ |
CFR Regulation Number | 888.3520 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-08-01 |
Decision Date | 2008-11-28 |
Summary: | summary |