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FDA 510(k)

EXPENDAGUIDE MULTIPLE HIP PINNING GUIDE SYSTEM

K-Number: K862279 · 1986-07-25

ApplicantOrthospec, Inc.
Decision Date1986-07-25
Product CodeKTW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EXPENDAGUIDE MULTIPLE HIP PINNING GUIDE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Orthospec, Inc.. It received FDA 510(k) clearance on 1986-07-25 under 510(k) number K862279. The device is classified under product code KTW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXPENDAGUIDE MULTIPLE HIP PINNING GUIDE SYSTEM?

EXPENDAGUIDE MULTIPLE HIP PINNING GUIDE SYSTEM is a medical device that received FDA 510(k) clearance on 1986-07-25. The listed applicant is Orthospec, Inc.. The 510(k) number is K862279.

When did EXPENDAGUIDE MULTIPLE HIP PINNING GUIDE SYSTEM receive FDA 510(k) clearance?

EXPENDAGUIDE MULTIPLE HIP PINNING GUIDE SYSTEM received FDA 510(k) clearance on 1986-07-25, under 510(k) number K862279.

Who is the listed applicant for EXPENDAGUIDE MULTIPLE HIP PINNING GUIDE SYSTEM?

The FDA 510(k) record lists Orthospec, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXPENDAGUIDE MULTIPLE HIP PINNING GUIDE SYSTEM?

The FDA product code for EXPENDAGUIDE MULTIPLE HIP PINNING GUIDE SYSTEM is KTW.

Related Clinical Trials

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Related Devices (Code: KTW)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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