KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A
K-Number: K032212 · 2003-09-15
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Device Summary
Frequently Asked Questions
What is the KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A?
KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A is a medical device that received FDA 510(k) clearance on 2003-09-15. The listed applicant is Kyphon, Inc.. The 510(k) number is K032212.
When did KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A receive FDA 510(k) clearance?
KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A received FDA 510(k) clearance on 2003-09-15, under 510(k) number K032212.
Who is the listed applicant for KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A?
The FDA 510(k) record lists Kyphon, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A?
The FDA product code for KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A is HRX.
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 Kyphon, 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: HRX)
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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