AD-TECH'S SPINAL ELECTRODE
K-Number: K973454 · 1998-06-10
Advertisement
Device Summary
Frequently Asked Questions
What is the AD-TECH'S SPINAL ELECTRODE?
AD-TECH'S SPINAL ELECTRODE is a medical device that received FDA 510(k) clearance on 1998-06-10. The listed applicant is Ad-Tech Medical Instrument Corp. The 510(k) number is K973454.
When did AD-TECH'S SPINAL ELECTRODE receive FDA 510(k) clearance?
AD-TECH'S SPINAL ELECTRODE received FDA 510(k) clearance on 1998-06-10, under 510(k) number K973454.
Who is the listed applicant for AD-TECH'S SPINAL ELECTRODE?
The FDA 510(k) record lists Ad-Tech Medical Instrument Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AD-TECH'S SPINAL ELECTRODE?
The FDA product code for AD-TECH'S SPINAL ELECTRODE is GZL.
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.
Other records listing Ad-Tech Medical Instrument Corp 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.
Related Devices (Code: GZL)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement