Atlas FDA

RESTORIS Multicompartmental Knee System

FDA 510(k) clearance K150307 · decided 2015-03-10

Clearance details

K-number
K150307
Device name
RESTORIS Multicompartmental Knee System
Applicant
Mako Surgical Corp.
Decision
Substantially Equivalent
Date received
2015-02-09
Decision date
2015-03-10
Days to decision
29 days
Clearance type
Special
Product code
NPJ
Device class
2
Regulation number
888.3560
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Fort Lauderdale, FL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
RESTORIS MULTICOMPARTMENTAL KNEE SYSTEM (K133039)Mako Surgical Corporation2013-12-10
IDUO BICOMPARTMENTAL KNEE REPAIR SYSTEM (K093513)Conformis, Inc.2009-12-16
SMITH & NEPHEW, INC. JOURNEY SELECT KNEE SYSTEM (K093056)Smith & Nephew, Inc.2009-12-15
RESTORIS MULTICOMPARTMENTAL KNEE (MCK) SYSTEM (K090763)Mako Surgical Corporation2009-06-17
DEPUY GCK FEMORAL AND TIBIAL COMPONENTS (K070849)DePuy Orthopaedics, Inc.2007-06-26
DEPUY GRADUATED COMPARTMENTAL KNEE (GCK) (K061648)DePuy Orthopaedics, Inc.2006-09-11
SMITH & NEPHEW COMPETITOR DEUCE FEMORAL COMPONENTS (K061569)Smith & Nephew, Inc.2006-07-06
CONFORMIS BICOMPARTMENTAL KNEE REPAIR SYSTEM (K053488)Conformis, Inc.2006-03-09
SMITH & NEPHEW COMPETITOR DUO KNEE FEMORAL (K052265)Smith & Nephew, Inc.2005-12-27
STRYKER COMPARTMENTAL KNEE SYSTEM (K052917)Howmedica Osteonics Corp.2005-12-27
SMITH & NEPHEW HYBRID KNEE FEMORAL (K042896)Smith & Nephew, Inc.2005-01-12

Recalls involving this device

No recalls on record reference this clearance.