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FDA 510(k)

CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS)

K-Number: K002693 · 2000-11-09

Decision Date2000-11-09
Product CodeEBL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS) is the device name listed in this FDA 510(k) record. The listed applicant is Cbs Intl. B.V.. It received FDA 510(k) clearance on 2000-11-09 under 510(k) number K002693. The device is classified under product code EBL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS)?

CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS) is a medical device that received FDA 510(k) clearance on 2000-11-09. The listed applicant is Cbs Intl. B.V.. The 510(k) number is K002693.

When did CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS) receive FDA 510(k) clearance?

CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS) received FDA 510(k) clearance on 2000-11-09, under 510(k) number K002693.

Who is the listed applicant for CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS)?

The FDA 510(k) record lists Cbs Intl. B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS)?

The FDA product code for CBW BRIDGE SYSTEM (CONSISTING OF CBW ANDCHORS, CBW MICRO-HANDPIECE AND BURS) is EBL.

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.

Related Devices (Code: EBL)

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.

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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