FDA.reportPublic FDA data

510(k) K221220

Device
Montross Extremity Medical Hemi Implant System
Applicant
Montross Extremity Medical
510(k) number
K221220
Product code
KWD
Decision
Substantially Equivalent (SESE)
Decision date
2023-04-19
Date received
2022-04-27
Regulation
888.3730
Classification name
Prosthesis, Toe, Hemi-, Phalangeal
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
William Montross
Address
20 Belle Air Rd. Colorado Springs CO US 80906 80906

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code KWD#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K250074HYALEX® MTP Hemiarthroplasty ImplantHyalex Orthopaedics, Inc.2026-04-03
K240268Accu-Joint Hemi ImplantAccufix Surgical, Inc.2024-02-29
K222964BioPoly Lesser Toe Hemiarthroplasty ImplantBioPoly, LLC2022-11-22
K201393restor3d MTP ImplantRestor3D, Inc.2022-05-25
K203634BioPoly Great Toe Hemiarthroplasty ImplantBioPoly, LLC2021-02-02
K200951Accu-Joint Hemi ImplantAccufix Surgical, Inc.2020-12-08
K190261BOSS Toe Fixation SystemArthrosurface, Inc.2019-08-14
K190543Cannulated Hemi ImplantVilex IN Tennessee, Inc.2019-05-31
K161279Life Spine Metatarsal Hemi ImplantLife Spine, Inc.2017-02-01
K152454HemiCAP MTP Resurfacing Hemi-Arthroplasty SystemArthrosurface, Inc.2016-04-11
K131377HEMICAP MTP RESURFACING HEMI-ARTHROPLASTY IMPLANTArthrosurface, Inc.2013-11-19
K131187LESSER METATARSAL HEAD IMPLANT SYSTEMSolana Surgical, LLC2013-10-22
K121973BIOPRO HEMI-EDGE TOE SYSTEMBiopro, Inc.2012-10-30
K113752METATARSAL DECOMPRESSION IMPLANT SURGICAL INSTRUMENT SETSolana Surgical, LLC2012-02-06
K120029HEMI PHALANGEAL IMPLANT SURGICAL INSTRUMENT SETSolana Surgical, LLC2012-02-06