SYNTHES ANATOMICAL LOCKING PLATE SYSTEM
K-Number: K961413 · 1996-08-07
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Device Summary
Frequently Asked Questions
What is the SYNTHES ANATOMICAL LOCKING PLATE SYSTEM?
SYNTHES ANATOMICAL LOCKING PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 1996-08-07. The listed applicant is Synthes (Usa). The 510(k) number is K961413.
When did SYNTHES ANATOMICAL LOCKING PLATE SYSTEM receive FDA 510(k) clearance?
SYNTHES ANATOMICAL LOCKING PLATE SYSTEM received FDA 510(k) clearance on 1996-08-07, under 510(k) number K961413.
Who is the listed applicant for SYNTHES ANATOMICAL LOCKING PLATE SYSTEM?
The FDA 510(k) record lists Synthes (Usa) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTHES ANATOMICAL LOCKING PLATE SYSTEM?
The FDA product code for SYNTHES ANATOMICAL LOCKING PLATE SYSTEM is HWC. This falls under the Cardiovascular category.
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 Synthes (Usa) 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: HWC)
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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