Meridian St Femoral Stem and Vitalock Solid Back Shell W/ Peri-Apatite Coating

• • Terminated Z-0107-06 FDA Unclassified (pre-2012) ·initiated 24 Aug 2005 ·on shared 510(k) K971206

  The V40 femoral head may not properly engage on the referenced V40 cobal chrome femoral hip stems.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

510(k) Number

K971206 ↗

FDA Product Code

LPH

Device Class

Class II

Regulation

21 CFR Part 888.3358

Advisory Committee

Orthopedic

FDA Decision

SN

• Howmedica(R) Fully Threaded Screws

  Class II

  FDA 510(k) K974720 Active Cleared 13 Mar 1998

• Alta Femoral Intramedullary Rods/Cfx Rods Modification

  Class II

  FDA 510(k) K935295 Active Cleared 11 Oct 1994

• Naso-Gard Nasogastric Tube Holder

  Class II

  FDA 510(k) K801511 Active Cleared 28 Jul 1980

• Class of Casting Alloys Type III or Alt

  Class II

  FDA 510(k) K820434 Active Cleared 11 Mar 1982

• Howmedica Zirconia Ceramic Femoral Head

  Class II

  FDA 510(k) K945090 Active Cleared 19 Jan 1995

• Extended Balljoint Grip

  Class II

  FDA 510(k) K802723 Active Cleared 19 Nov 1980

See all devices from Howmedica Corp. →