Skip to content

A Caliper

by Twin City Surgical, Inc. 510(k)

Active United States

510(k) K820659

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK820659 Date19 Mar 1982ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
KTZ
Device Class
Class I
Regulation
21 CFR Part 888.4150
Advisory Committee
Orthopedic
FDA Decision
SESE Substantially Equivalent

Other devices from Twin City Surgical, Inc.

  • Sims Chair

    Class II

  • Spinal Wrench

    Class I

  • Anvil Retractor

    Class I

  • The (Crom) Tester

    Class I

  • A Hook Driver

    Class II