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FDA 510(k)

COPSIOS BONE VOID FILLER (BVF)

K-Number: K033679 · 2004-07-07

ApplicantCenterpulse Spine-Tech, Inc.
Decision Date2004-07-07
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COPSIOS BONE VOID FILLER (BVF) is the device name listed in this FDA 510(k) record. The listed applicant is Centerpulse Spine-Tech, Inc.. It received FDA 510(k) clearance on 2004-07-07 under 510(k) number K033679. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COPSIOS BONE VOID FILLER (BVF)?

COPSIOS BONE VOID FILLER (BVF) is a medical device that received FDA 510(k) clearance on 2004-07-07. The listed applicant is Centerpulse Spine-Tech, Inc.. The 510(k) number is K033679.

When did COPSIOS BONE VOID FILLER (BVF) receive FDA 510(k) clearance?

COPSIOS BONE VOID FILLER (BVF) received FDA 510(k) clearance on 2004-07-07, under 510(k) number K033679.

Who is the listed applicant for COPSIOS BONE VOID FILLER (BVF)?

The FDA 510(k) record lists Centerpulse Spine-Tech, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COPSIOS BONE VOID FILLER (BVF)?

The FDA product code for COPSIOS BONE VOID FILLER (BVF) is MQV.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Centerpulse Spine-Tech, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K031511DYNESYS SPINAL SYSTEMK022615CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTORK022344TRINICA SELECT ANTERIOR CERVICAL PLATE SYSTEM

Related Devices (Code: MQV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262230Mg OSTEOREVIVE™;Mg OSTEOCRETE™Bone Solutions, Inc.K260364Device 300419 StripGeistlich Pharma AGK252797JAZBI™ Resorbable Bone Void FillerSdip Innovations Pty, Ltd.K261008Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive Bone Graft Substitute; Vitoss BBTrauma® Bioactive Bone Graft Substitute; Vitoss® BA2X Bioactive Bone Graft Substitute; Vitoss® Bioactive Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft SubstituteStryker SpineK253524Adaptos®Fuse Bone GraftBiomendex OYK253147FIBERGRAFT™ BG Putty GPS Bone Graft Substitute FIBERGRAFT™ BG Putty Bone Graft Substitute FIBERGRAFT™ AERIDYAN™ Matrix Bone Graft Substitute FIBERGRAFT™ BG Matrix Bone Graft SubstituteProsidyan, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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