FDA device listing

ENDOBUTTON,ROUND ENDOBUTTON 1-HOLE SST FOR SZ3/4 SUTURE LOOP,ROUND ENDOBUTTON 2-HOLE SST,ROUND ENDOBUTTON 2-HOLE WITH…

FDA device listing 1681942309 · Smith & Nephew, Inc.

Key facts

Proprietary names ENDOBUTTON,ROUND ENDOBUTTON 1-HOLE SST FOR SZ3/4 SUTURE LOOP,ROUND ENDOBUTTON 2-HOLE SST,ROUND ENDOBUTTON 2-HOLE WITH POST SST WITH SZ3/4 SUTURE LOOP,ROUND ENDOBUTTON 2-HOLE W/POST SST
Owner/operator Smith & Nephew, Inc.
Owner/operator number 1020279
Premarket submissions K183232
Product codes HTN, HWC
Device names HTN - Washer, Bolt Nut, HWC - Screw, Fixation, Bone
Device class Class II
Classification regulations (21 CFR) 888.3030, 888.3040
Review panels Orthopedic
Registered establishments SMITH & NEPHEW INC.
Establishment registrations 1219602, 1643264, 3003604053
FEI numbers 1219602, 1643264, 3003604053
Establishment operations Manufacturer, Specification Developer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 1–9 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

Browse all FDA device listings