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FDA 510(k)

S-BONE HIP TOOL

K-Number: K052538 · 2005-10-07

Decision Date2005-10-07
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

S-BONE HIP TOOL is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Sciences, Inc.. It received FDA 510(k) clearance on 2005-10-07 under 510(k) number K052538. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S-BONE HIP TOOL?

S-BONE HIP TOOL is a medical device that received FDA 510(k) clearance on 2005-10-07. The listed applicant is Orthopedic Sciences, Inc.. The 510(k) number is K052538.

When did S-BONE HIP TOOL receive FDA 510(k) clearance?

S-BONE HIP TOOL received FDA 510(k) clearance on 2005-10-07, under 510(k) number K052538.

Who is the listed applicant for S-BONE HIP TOOL?

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

What is the FDA product code for S-BONE HIP TOOL?

The FDA product code for S-BONE HIP TOOL is HRS.

Other records listing Orthopedic Sciences, 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.

View all 10 devices →

Related Devices (Code: HRS)

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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