# Zimmer Trabecular Metal Technology

- Location (FDA's records): Parsippany, NJ
- FDA decisions: 13 (2007–2014): 13 510(k) clearances
- Names in FDA's records: Zimmer Trabecular Metal Technology (11); Zimmer Trabecular Metal Technology, Inc. (2)
- Product codes: MBH (3), ODP (3), MAX (3), MQP (3), KWS (1)
- Predicates its devices cite: 39 (10 its own); citations of its devices by later devices: 42 (10 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Implex Corp.: 13 (https://510kreport.com/company/implex)
- Zimmer Trabecular: 5 (https://510kreport.com/company/zimmer-trabecular)
- Spinal Elements, Inc.: 2 (https://510kreport.com/company/spinal-elements)
- Abbott Spine, Inc.: 2 (https://510kreport.com/company/abbott-spine)
- Alphatec Spine, Inc.: 1 (https://510kreport.com/company/alphatec-spine)
- Sulzer Spine-Tech: 1 (https://510kreport.com/company/sulzer-spine-tech)
- Medtronic Sofamor Danek USA, Inc.: 1 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Biomet Spine: 1 (https://510kreport.com/company/biomet-spine)

## Firms that cite its devices most
- Zimmer Spine, Inc.: 7 (https://510kreport.com/company/zimmer-spine)
- Lima Corporate S.P.A.: 3 (https://510kreport.com/company/lima-corporate)
- Zimmer, Inc.: 3 (https://510kreport.com/company/zimmer)
- Medacta International S.A.: 2 (https://510kreport.com/company/medacta-international)
- Waldemar Link GmbH & Co. KG: 2 (https://510kreport.com/company/waldemar-link)
- Lntelivation, LLC: 2 (https://510kreport.com/company/lntelivation)
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)
- Shenzhen Dazhou Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-dazhou-medical-technology)

## Its most-cited devices
- K103033: Trabecular Metal Fusion Device Model 06-101-Xxxxx, 06-102-Xxxxx and 08-100-Xxxxx (2011), cited by 8
- K102896: Trabecular Metal Tibial Cone Augments (2010), cited by 7
- K113561: TM Ardis Interbody System TM Ardis Interbody System Instrumenation (2012), cited by 6
- K111983: Vista-S Device Model 08/06-401-Xxxxx, 08/06-402-Xxxxxx (2011), cited by 4
- K103517: Trabecular Metal Femoral Cone Augments (2011), cited by 4
- K133784: Vista-S Device, Associated Instrumentation (2014), cited by 3

## Recent decisions
- K133784: Vista-S Device, Associated Instrumentation (Jul 7, 2014)
- K123602: TM Ardis Interbody System Inserter (Mar 1, 2013)
- K120990: Nexgen LCCK Trabecular Metal (TM) Coupled Tibial Cones Provisionals to Nexgen LCCK Trabecular Metal (TM) Coupled Tibial (Jun 29, 2012)
- K120203: TM-400 Device (Jun 15, 2012)
- K113561: TM Ardis Interbody System TM Ardis Interbody System Instrumenation (May 29, 2012)
- K111983: Vista-S Device Model 08/06-401-Xxxxx, 08/06-402-Xxxxxx (Nov 18, 2011)
- K103517: Trabecular Metal Femoral Cone Augments (Feb 15, 2011)
- K103033: Trabecular Metal Fusion Device Model 06-101-Xxxxx, 06-102-Xxxxx and 08-100-Xxxxx (Jan 10, 2011)

Source page: https://510kreport.com/company/zimmer-trabecular-metal-technology