Tsrh Anterior Spinal Screws, Staples and End Plate

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K883784 ↗

FDA Product Code

LYQ

Device Class

Class I

Regulation

21 CFR Part 888.4540

Advisory Committee

Orthopedic

FDA Decision

SN

• Cradle, Hospital Bed Clothing

  Class I

  FDA 510(k) K892877 Active Cleared 15 Jun 1989

• Interlocking Femoral Nail(Left & Right) Tibial Nai

  Class II

  FDA 510(k) K852020 Active Cleared 22 May 1985

• Schultz Phalangeal Component Driver

  Class I

  FDA 510(k) K870847 Active Cleared 13 Mar 1987

• Warsaw Orthopedic I Bone Plate

  Class II

  FDA 510(k) K870727 Active Cleared 9 Mar 1987

• Schultz Metacarpophalangeal Joint Prosthesis

  Not classified

  FDA 510(k) K860074 Active Cleared 11 Feb 1986

• Fixation Staple Driver/Extractor

  Class II

  FDA 510(k) K832884 Active Cleared 20 Oct 1983

See all devices from Warsaw Orthopedic, Inc. →