STACKABLE CAGE SYSTEM

Spinal Vertebral Body Replacement Device

DEPUY ACROMED

The following data is part of a premarket notification filed by Depuy Acromed with the FDA for Stackable Cage System.

Pre-market Notification Details

• Device ID: K001340
• 510k Number: K001340
• Device Name: STACKABLE CAGE SYSTEM
• Classification: Spinal Vertebral Body Replacement Device
• Applicant: DEPUY ACROMED 325 PARAMOUNT DR. Raynham, MA 02767 -0350
• Contact: Karen Jurczak
• Correspondent: Karen Jurczak; DEPUY ACROMED 325 PARAMOUNT DR. Raynham, MA 02767 -0350
• Product Code: MQP
• CFR Regulation Number: 888.3060 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2000-04-27
• Decision Date: 2000-07-26

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
10705034017273	K001340	000
10705034017082	K001340	000
10705034017075	K001340	000
10705034017068	K001340	000
10705034017051	K001340	000
10705034017044	K001340	000
10705034017037	K001340	000
10705034017013	K001340	000
10705034016993	K001340	000
10705034016986	K001340	000
10705034016979	K001340	000
10705034016962	K001340	000
10705034016955	K001340	000
10705034016948	K001340	000
10705034246994	K001340	000
10705034017099	K001340	000
10705034017105	K001340	000
10705034017259	K001340	000
10705034017235	K001340	000
10705034017396	K001340	000
10705034017389	K001340	000
10705034017372	K001340	000
10705034017365	K001340	000
10705034017020	K001340	000
10705034017174	K001340	000
10705034017167	K001340	000
10705034017150	K001340	000
10705034017143	K001340	000
10705034017136	K001340	000
10705034017129	K001340	000
10705034017112	K001340	000
10705034246932	K001340	000