CUTTER, P606 BONE
K-Number: K770302 · 1977-03-09
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Device Summary
Frequently Asked Questions
What is the CUTTER, P606 BONE?
CUTTER, P606 BONE is a medical device that received FDA 510(k) clearance on 1977-03-09. The listed applicant is Dentronix, Inc.. The 510(k) number is K770302.
When did CUTTER, P606 BONE receive FDA 510(k) clearance?
CUTTER, P606 BONE received FDA 510(k) clearance on 1977-03-09, under 510(k) number K770302.
Who is the listed applicant for CUTTER, P606 BONE?
The FDA 510(k) record lists Dentronix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CUTTER, P606 BONE?
The FDA product code for CUTTER, P606 BONE is FZT.
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 Dentronix, 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.
Related Devices (Code: FZT)
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.
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