FDA 510(k)

LIGHT SABRE SPINAL ACCESS DEVICE

K-Number: K071814 · 2007-10-16

Decision Date2007-10-16

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

LIGHT SABRE SPINAL ACCESS DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Minrad, Inc.. It received FDA 510(k) clearance on 2007-10-16 under 510(k) number K071814. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHT SABRE SPINAL ACCESS DEVICE?

LIGHT SABRE SPINAL ACCESS DEVICE is a medical device that received FDA 510(k) clearance on 2007-10-16. The listed applicant is Minrad, Inc.. The 510(k) number is K071814.

When did LIGHT SABRE SPINAL ACCESS DEVICE receive FDA 510(k) clearance?

LIGHT SABRE SPINAL ACCESS DEVICE received FDA 510(k) clearance on 2007-10-16, under 510(k) number K071814.

Who is the listed applicant for LIGHT SABRE SPINAL ACCESS DEVICE?

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

What is the FDA product code for LIGHT SABRE SPINAL ACCESS DEVICE?

The FDA product code for LIGHT SABRE SPINAL ACCESS DEVICE is KNW.

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Other records listing Minrad, Inc. as applicant

K072255MINRAD INC. NASAL SCAVENGING CIRCUIT K062231MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001 K062230MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002 K041852MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002 K041846SABRESOURCE DRAPE K021084LIGHT SABER SPINAL NEEDLE

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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.