Atlas FDA

ACUMED ANATOMIC RADIAL HEAD SYSTEM

FDA 510(k) clearance K041858 · decided 2004-10-05

Clearance details

K-number
K041858
Device name
ACUMED ANATOMIC RADIAL HEAD SYSTEM
Applicant
Acumed, LLC
Decision
Substantially Equivalent
Date received
2004-07-09
Decision date
2004-10-05
Days to decision
88 days
Clearance type
Traditional
Product code
KWI
Device class
2
Regulation number
888.3170
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Hillsboro, OR, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Arthrex Radial Head Replacement System (K260624)Arthrex, Inc.2026-07-30
BioPoly Radial Head Implant (K233592)BioPoly, LLC2024-03-13
ALIGN Radial Head System (K231188)Skeletal Dynamics, Inc.2023-09-28
DePuy Synthes Radial Head Replacement System (K213563)DePuy Synthes2022-03-18
Avenger Radial Head System (K212872)In2bones USA, LLC2021-12-17
Avenger Radial Head System (K192754)In2bones USA, LLC2020-01-07
Revolution Radial Head (K183618)Ignite Orthopedics, Inc.2019-05-17
Align Radial Head System (K172688)Skeletal Dynamics, LLC2017-12-22
AXIA RADIAL HEAD SYSTEM (K132735)Imds (Innovative MEdical Device Systems) - Leis ME2014-01-07
ACUMED ANATOMIC RADIAL HEAD SYSTEM, ACUMED ANATOMIC RADIAL HEAD LONG STEMS, ACUMED ARH SLIDE-LOC (K131845)Acumed, LLC2013-09-30
SYNTHES RADIAL HEAD PROSTHESIS SYSTEM (K112030)Synthes USA, LLC2012-06-19
ALIGN RADIAL HEAD SYSTEM (K092721)Skeletal Dynamics, LLC2010-08-03

Recalls involving this device

No recalls on record reference this clearance.