FDA 510(k)

SMITH AND NEPHEW SPINE DEFLECTING FORCEPS

K-Number: K940222 · 1994-06-29

Decision Date1994-06-29

Product CodeHRX

Advisory CommitteeOR

DecisionSubstantially Equivalent for Some Indications

Device Summary

SMITH AND NEPHEW SPINE DEFLECTING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 1994-06-29 under 510(k) number K940222. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the SMITH AND NEPHEW SPINE DEFLECTING FORCEPS?

SMITH AND NEPHEW SPINE DEFLECTING FORCEPS is a medical device that received FDA 510(k) clearance on 1994-06-29. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K940222.

When did SMITH AND NEPHEW SPINE DEFLECTING FORCEPS receive FDA 510(k) clearance?

SMITH AND NEPHEW SPINE DEFLECTING FORCEPS received FDA 510(k) clearance on 1994-06-29, under 510(k) number K940222.

Who is the listed applicant for SMITH AND NEPHEW SPINE DEFLECTING FORCEPS?

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

What is the FDA product code for SMITH AND NEPHEW SPINE DEFLECTING FORCEPS?

The FDA product code for SMITH AND NEPHEW SPINE DEFLECTING FORCEPS is HRX.

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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.