Lsf(Tm) Total Hip System

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K901460 ↗

FDA Product Code

JDI

Device Class

Class II

Regulation

21 CFR Part 888.3350

Advisory Committee

Orthopedic

FDA Decision

SN

• LSF HA Coated Femoral Hip

  Class II

  FDA 510(k) K915617 Active Cleared 28 May 1992

• Lsf Cemented Femoral Hip

  Class II

  FDA 510(k) K902727 Active Cleared 9 Aug 1990

• Communitrach Tube

  Class II

  FDA 510(k) K823291 Active Cleared 8 Jan 1983

• Implant Technology Bone Cement Extractor

  Class II

  FDA 510(k) K891472 Active Cleared 2 May 1989

• Communi-Trach Tube

  Class II

  FDA 510(k) K841546 Active Cleared 30 Apr 1984

• Lsf Total Hip System - Muller-Type Acetabular Cup

  Class II

  FDA 510(k) K920021 Active Cleared 25 Mar 1992

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