Anterior Spine System
FDA 510(k) K934429 · Buckman Co., Inc.
510(k) numberK934429
Submission
- Device name
- Anterior Spine System
- Applicant
- Buckman Co., Inc.
Concord, CA, US - Received
- September 13, 1993
- Decision date
- October 20, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KWQ – Appliance, Fixation, Spinal Intervertebral Body
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3060
- Specialty
- Orthopedic
- Implant
- Yes
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| K252776 | ARIES Anterior Cervical Plate SystemsKWQ · Traditional | ZheJiang Decans Medical Devices Co., Ltd. | 05/14/2026SE |
| K261112 | CastleLoc-P Anterior Cervical Plate SystemKWQ · Special | L&K BIOMED Co., Ltd. | 05/06/2026SE |
| K260570 | corra cervical plating systemKWQ · Traditional | Carlsmed, Inc. | 04/22/2026SE |
| K260697 | VyPlate Anterior Cervical Plate SystemKWQ · Special | Vy Spine, LLC | 03/27/2026SE |
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| K251940 | PathLoc Lumbar Plate SystemKWQ · Traditional | L&K BIOMED Co., Ltd. | 03/03/2026SE |
| K254182 | AsterKWQ · Traditional | Osteonic Co., Ltd. | 02/26/2026SE |
| K253201 | Lumbar Spine Truss System - Plating Solution (LSTS-PS)KWQ · Special | 4Web, Inc. | 02/12/2026SE |
| K252611 | aprevo® cervical plating systemKWQ · Traditional | Carlsmed, Inc. | 12/22/2025SE |
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| K964252 | OrthochuckGEY · Traditional | 05/27/1997SE |
| K950099 | Synergy(Tm) Ti Posterior Spinal SystemMNH · Traditional | 01/16/1997SN |
| K960451 | Webb-Morley Spine SystemMNH · Traditional | 04/18/1996SN |
| K950999 | KSF Posterior Spingal Fixator for Severe SpondylolisthesisMNH · Traditional | 01/25/1996SE |
| K945756 | Imagn(Tm) 2000 SystemGKZ · Traditional | 12/19/1995SE |
| K940003 | Volumet CD4 + and CD8 + T Lymphocyte Count Test KitGKZ · Traditional | 10/19/1995SE |
| K951117 | Lihtan 532 LaserGEX · Traditional | 10/18/1995SE |
| K942751 | Vanguard Series Gas RegulatorsCAN · Traditional | 02/09/1995SE |
Questions and answers
When was Anterior Spine System cleared by the FDA?
Anterior Spine System (K934429) received a 510(k) decision of Substantially Equivalent on October 20, 1994, 402 days after the submission was received.
What is the product code of K934429?
The FDA product code is KWQ – Appliance, Fixation, Spinal Intervertebral Body, a Class II (moderate risk) device regulated under 21 CFR 888.3060.