The following data is part of a premarket notification filed by Mako Surgical Corp. with the FDA for Robotic Arm Interactive Orthopedic System-hip.
Device ID | K091998 |
510k Number | K091998 |
Device Name: | ROBOTIC ARM INTERACTIVE ORTHOPEDIC SYSTEM-HIP |
Classification | Orthopedic Stereotaxic Instrument |
Applicant | MAKO SURGICAL CORP. 2555 DAVIE RD., SUITE 110 Ft. Lauderdale, FL 33317 |
Contact | William Tapia |
Correspondent | William Tapia MAKO SURGICAL CORP. 2555 DAVIE RD., SUITE 110 Ft. Lauderdale, FL 33317 |
Product Code | OLO |
CFR Regulation Number | 882.4560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-07-02 |
Decision Date | 2009-09-28 |
Summary: | summary |