Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3039167712

FEI Number

3039167712

Entity Name

FOUNDATION SURGICAL GROUP

City/State/Country

Scottsdale, AZ, US

Establishment Address

7327 E Tierra Buena Ln Ste 101, Scottsdale, AZ 85260, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Foundation Surgical Group (Owner Number: 10093677)

Owner / Operator Contact Address

7327 E Tierra Buena Lane, Suite 101, Scottsdale, AZ 85260, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K241468

PMA Number

N/A

All Registered Proprietary Names

Interwedge Vertiwedge

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MAX	Intervertebral Fusion Device With Bone Graft, Lumbar	Orthopedic	Class 2	888.3080	2025-06-20
OVD	Intervertebral Fusion Device With Integrated Fixation, Lumbar	Orthopedic	Class 2	888.3080	2025-06-20
MQP	Spinal Vertebral Body Replacement Device	Orthopedic	Class 2	888.3060	2025-06-20

Official Correspondent

Christopher Reah

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Foundation Surgical Group

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K223430	Life Spine, Inc.	ProLift Micro Expandable Spacer System	2023-05-04
K102293	Globus Medical, Inc.	CALIBER SPACER	2011-01-05
K193541	Nu Vasive, Incorporated	NuVasive Cohere Thoracolumbar Interbody System	2020-03-30
K080401	Advanced Medical Technologies AG	SHELL CAGE, WAVE CAGE, LOOP CAGE	2008-05-09
K200084	Zavation Medical Products, LLC	Zavation IBF System	2020-10-19

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3039167712. Last updated year: 2026. Please use registration number 3039167712 when referencing this establishment in official correspondence.