SYNTHES PANGEA MONOAXIAL SYSTEM— 510(k) K052151

Substantially Equivalent

Synthes Spine Co.Lp

FDA 510(k) clearance K052151 for SYNTHES PANGEA MONOAXIAL SYSTEM, Substantially Equivalent on 2005-12-07. Applicant: Synthes Spine Co.Lp.

Clearance details

Applicant: Synthes Spine Co.Lp
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2005-08-08
Decision date: 2005-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Chester, PA, US

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Adverse events under product code NKB

product code NKB

Death: 27
Injury: 5,033
Malfunction: 4,140
Total: 9,200

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.