AccessGUDID - DEVICE: Arcos® One-Piece Revision System (00887868469510)

GUDID

Device Identifier (DI) Information

Brand Name: Arcos® One-Piece Revision System
Version or Model: 110024885
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 110024885
Company Name: Biomet Orthopedics, LLC

Primary DI Number: 00887868469510
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 129278169 *Terms of Use

Device Description: No description.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
58481	Femoral stem prosthesis trial	A copy of a final femoral stem prosthesis designed to be used for trial reductions during hip arthroplasty to judge the correct offset, leg-length, and range of motion of the final femoral prosthesis to be implanted. It is one of a set, or a set, of graduated sizes, and is used in conjunction with femoral head trial prostheses. It is typically made of metal or polymer material and includes trial stems, trial sleeves, and trial necks. This is a reusable device intended to be sterilized prior to use.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
PBI	prosthesis, hip, constrained, cemented or uncemented, metal/polymer, + additive
OQI	Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented
KWZ	Prosthesis, hip, constrained, cemented or uncemented, metal/polymer
JDI	Prosthesis, hip, semi-constrained, metal/polymer, cemented
KWL	Prosthesis, hip, hemi-, femoral, metal
OQH	Hip, semi-constrained, cemented, metal/polymer + additive, cemented
LPH	PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
OQG	Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented
LWJ	Prosthesis, hip, semi-constrained, metal/polymer, uncemented
KWY	Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented
LZO	Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K151603	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: Sizes 15 - 18

Device Record Status

Public Device Record Key: 109b6ef2-3b57-43a3-aedb-8439b79cf111
Public Version Date: May 30, 2025
Public Version Number: 2
DI Record Publish Date: April 23, 2022