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FDA 510(k)

KYPHON INFLATABLE BONE TAMP

K-Number: K981251 · 1998-07-02

ApplicantKyphon, Inc.
Decision Date1998-07-02
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KYPHON INFLATABLE BONE TAMP is the device name listed in this FDA 510(k) record. The listed applicant is Kyphon, Inc.. It received FDA 510(k) clearance on 1998-07-02 under 510(k) number K981251. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KYPHON INFLATABLE BONE TAMP?

KYPHON INFLATABLE BONE TAMP is a medical device that received FDA 510(k) clearance on 1998-07-02. The listed applicant is Kyphon, Inc.. The 510(k) number is K981251.

When did KYPHON INFLATABLE BONE TAMP receive FDA 510(k) clearance?

KYPHON INFLATABLE BONE TAMP received FDA 510(k) clearance on 1998-07-02, under 510(k) number K981251.

Who is the listed applicant for KYPHON INFLATABLE BONE TAMP?

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 KYPHON INFLATABLE BONE TAMP?

The FDA product code for KYPHON INFLATABLE BONE TAMP is HRX.

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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.

K073516DISCYPHOR DIRECT CATHETER SYSTEM, DISCYPHOR DIRECT NEEDLES, LONG, DISCYPHOR DIRECT NEEDLES, REGULARK063071DISCYPHOR CATHETER SYSTEM, MODEL D01A; DISCYPHOR INTRODUCER NEEDLE, MODEL D01BK061210FUNCTIONAL ANAESTHETIC DISCOGRAPHY (FAD) CATHETER SYSTEM, MODEL D01A ; INTRODUCER NEEDLE, MODEL D01BK041454KYPHX XPANDER INFLATABLE BONE TAMPS MODEL#KO8A,KO9A,K13AK041584KYPHX HV-R BONE CEMENT, MODEL C01AK033801KYPHX HV-R, MODEL C01A

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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.

K260203Fule Vertebroplasty Balloon CatheterBeijing Fule Science & Technology Development Co., Ltd.K254103HOPKINS Telescopes for ArthroscopyKarl Storz SE & CO. KGK252790Digital ClarusScope System and Digital NeuroPEN SystemClarus Medical, LLCK253523Freedom DS™ Decompression SystemSpinal SimplicityK252546VantageTM Lumbar Decompression KitAllevion Medical, LLCK253217MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700)Medimaging Integrated Solution, Inc (Miis)

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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