H-H HUNTER ACTIVE TENDON IMPLANT BC
K-Number: K872293 · 1987-09-28
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Device Summary
Frequently Asked Questions
What is the H-H HUNTER ACTIVE TENDON IMPLANT BC?
H-H HUNTER ACTIVE TENDON IMPLANT BC is a medical device that received FDA 510(k) clearance on 1987-09-28. The listed applicant is Holter-Hausner Intl.. The 510(k) number is K872293.
When did H-H HUNTER ACTIVE TENDON IMPLANT BC receive FDA 510(k) clearance?
H-H HUNTER ACTIVE TENDON IMPLANT BC received FDA 510(k) clearance on 1987-09-28, under 510(k) number K872293.
Who is the listed applicant for H-H HUNTER ACTIVE TENDON IMPLANT BC?
The FDA 510(k) record lists Holter-Hausner Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for H-H HUNTER ACTIVE TENDON IMPLANT BC?
The FDA product code for H-H HUNTER ACTIVE TENDON IMPLANT BC is HXA.
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 Holter-Hausner Intl. 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: HXA)
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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