RETROGRADE KNIFE, DISPOSABLE #TM-1613
K-Number: K873711 · 1987-11-02
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Device Summary
Frequently Asked Questions
What is the RETROGRADE KNIFE, DISPOSABLE #TM-1613?
RETROGRADE KNIFE, DISPOSABLE #TM-1613 is a medical device that received FDA 510(k) clearance on 1987-11-02. The listed applicant is Arthropedics, Inc.. The 510(k) number is K873711.
When did RETROGRADE KNIFE, DISPOSABLE #TM-1613 receive FDA 510(k) clearance?
RETROGRADE KNIFE, DISPOSABLE #TM-1613 received FDA 510(k) clearance on 1987-11-02, under 510(k) number K873711.
Who is the listed applicant for RETROGRADE KNIFE, DISPOSABLE #TM-1613?
The FDA 510(k) record lists Arthropedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RETROGRADE KNIFE, DISPOSABLE #TM-1613?
The FDA product code for RETROGRADE KNIFE, DISPOSABLE #TM-1613 is HTS.
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 Arthropedics, 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: HTS)
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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