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FDA 510(k)

S & S ORTHOPEDIC WIRE DRIVER 701

K-Number: K944488 · 1995-03-02

ApplicantS & S Orthopedic , Ltd.
Decision Date1995-03-02
Product CodeKIJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

S & S ORTHOPEDIC WIRE DRIVER 701 is the device name listed in this FDA 510(k) record. The listed applicant is S & S Orthopedic , Ltd.. It received FDA 510(k) clearance on 1995-03-02 under 510(k) number K944488. The device is classified under product code KIJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S & S ORTHOPEDIC WIRE DRIVER 701?

S & S ORTHOPEDIC WIRE DRIVER 701 is a medical device that received FDA 510(k) clearance on 1995-03-02. The listed applicant is S & S Orthopedic , Ltd.. The 510(k) number is K944488.

When did S & S ORTHOPEDIC WIRE DRIVER 701 receive FDA 510(k) clearance?

S & S ORTHOPEDIC WIRE DRIVER 701 received FDA 510(k) clearance on 1995-03-02, under 510(k) number K944488.

Who is the listed applicant for S & S ORTHOPEDIC WIRE DRIVER 701?

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

What is the FDA product code for S & S ORTHOPEDIC WIRE DRIVER 701?

The FDA product code for S & S ORTHOPEDIC WIRE DRIVER 701 is KIJ.

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Related Devices (Code: KIJ)

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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