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510(k) K150307

RESTORIS Multicompartmental Knee System by Mako Surgical Corp. — Product Code NPJ

K150307 is an FDA 510(k) premarket notification submitted by Mako Surgical Corp. for the device "RESTORIS Multicompartmental Knee System". The FDA issued a decision of Substantially Equivalent on March 10, 2015. The device falls under product code NPJ (Prosthesis, Knee Patellofemorotibial, Partial, Semi-Constrained, Cemented, Polymer/Metal/Polymer), a Class II device regulated under 21 CFR 888.3560. Mako Surgical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 10, 2015
Date Received
February 9, 2015
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Knee Patellofemorotibial, Partial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device Class
Class II
Regulation Number
888.3560
Review Panel
OR
Submission Type

The device is intended to replace the medial condyle and the patellofemoral compartment of the distal femur with a single device. The device is meant to be used with a uni-compartmental tibial base and insert and a resurfacing patella. The device is intended to be used with bone cement.

Other clearances by Mako Surgical Corp.

  • K260222 — Mako Total Knee Application (February 25, 2026)
  • K250608 — Mako Total Knee Application (3.0); Hybrid Tip Pointer (April 25, 2025)
  • K243751 — Mako Total Hip Application 5.0 (March 5, 2025)
  • K242373 — Mako Shoulder Application (1.0) (November 7, 2024)
  • K241011 — Mako Total Knee Application (June 11, 2024)
  • K220930 — Restoris Multi-Compartmental Knee System (June 2, 2022)
  • K220459 — Mako Total Knee Application (April 15, 2022)
  • K193515 — Mako Total Knee Application (July 14, 2020)
  • K193128 — Mako Total Hip Application (February 2, 2020)
  • K191998 — Mako Total Hip Application, Mako Total Knee Application (September 24, 2019)

Other clearances for product code NPJ

  • K133039 — RESTORIS MULTICOMPARTMENTAL KNEE SYSTEM (December 10, 2013)
  • K093513 — IDUO BICOMPARTMENTAL KNEE REPAIR SYSTEM (December 16, 2009)
  • K093056 — SMITH & NEPHEW, INC. JOURNEY SELECT KNEE SYSTEM (December 15, 2009)
  • K090763 — RESTORIS MULTICOMPARTMENTAL KNEE (MCK) SYSTEM (June 17, 2009)
  • K070849 — DEPUY GCK FEMORAL AND TIBIAL COMPONENTS (June 26, 2007)
  • K061648 — DEPUY GRADUATED COMPARTMENTAL KNEE (GCK) (September 11, 2006)
  • K061569 — SMITH & NEPHEW COMPETITOR DEUCE FEMORAL COMPONENTS (July 6, 2006)
  • K053488 — CONFORMIS BICOMPARTMENTAL KNEE REPAIR SYSTEM (March 9, 2006)
  • K052917 — STRYKER COMPARTMENTAL KNEE SYSTEM (December 27, 2005)
  • K052265 — SMITH & NEPHEW COMPETITOR DUO KNEE FEMORAL (December 27, 2005)

FDA data resources