LANCER PEDICLE SCREW SYSTEM— 510(k) K110633

Substantially Equivalent

Spinal Solutions, LLC

FDA 510(k) clearance K110633 for LANCER PEDICLE SCREW SYSTEM, Substantially Equivalent on 2011-12-15. Applicant: Spinal Solutions, LLC. Device class: 2.

Clearance details

Applicant
Spinal Solutions, LLC
Product code
Code MNH
Device class
Class 2
Regulation
21 CFR 888.3070
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Round Rock, TX, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code MNH

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Adverse events under product code MNH

product code MNH
Injury
978
Malfunction
793
Total
1,771

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 →

Recalls naming K110633

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K110633.

Data sourced from openFDA. This site is unofficial and independent of the FDA.