SYNTHES LOCKING CALCANEAL PLATES
K-Number: K991407 · 1999-06-11
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Device Summary
Frequently Asked Questions
What is the SYNTHES LOCKING CALCANEAL PLATES?
SYNTHES LOCKING CALCANEAL PLATES is a medical device that received FDA 510(k) clearance on 1999-06-11. The listed applicant is Synthes (Usa). The 510(k) number is K991407.
When did SYNTHES LOCKING CALCANEAL PLATES receive FDA 510(k) clearance?
SYNTHES LOCKING CALCANEAL PLATES received FDA 510(k) clearance on 1999-06-11, under 510(k) number K991407.
Who is the listed applicant for SYNTHES LOCKING CALCANEAL PLATES?
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 LOCKING CALCANEAL PLATES?
The FDA product code for SYNTHES LOCKING CALCANEAL PLATES is LXT.
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: LXT)
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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