HOURGLASS VERTEBRAL BODY SPACER— 510(k) K033926
Substantially EquivalentMedtronic Sofamor Danek
FDA 510(k) clearance K033926 for HOURGLASS VERTEBRAL BODY SPACER, Substantially Equivalent on 2004-07-07. Applicant: Medtronic Sofamor Danek. Device class: 2.
Clearance details
- Applicant
- Medtronic Sofamor Danek
- Product code
- Code MQP
- Device class
- Class 2
- Regulation
- 21 CFR 888.3060
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Memphis, TN, US
Recent devices under product code MQP
view allMore clearances from Medtronic Sofamor Danek
view all- K212428 — Centerpiece Plate Fixation System
- K201267 — Adaptix Interbody System with Titan nanoLOCK Surface Technology
- K173125 — T2 STRATOSPHERE Expandable Corpectomy System
- K172199 — ELEVATE Spinal System, CAPSTONE PTC Spinal System, CRESCENT Spinal System, CRESCENT Spinal System Titanium
- K171031 — CRESCENT Spinal System
Adverse events under product code MQP
product code MQP- Injury
- 372
- Malfunction
- 519
- Total
- 891
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.