FDA 510(k)

SURGICAL DYNAMICS DISCOGRAPHY SYSTEM

K-Number: K921950 · 1993-06-07

Decision Date1993-06-07

Product CodeFMI

Advisory CommitteeHO

DecisionUnknown

Device Summary

SURGICAL DYNAMICS DISCOGRAPHY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Dynamics, Inc.. It received FDA 510(k) clearance on 1993-06-07 under 510(k) number K921950. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SURGICAL DYNAMICS DISCOGRAPHY SYSTEM?

SURGICAL DYNAMICS DISCOGRAPHY SYSTEM is a medical device that received FDA 510(k) clearance on 1993-06-07. The listed applicant is Surgical Dynamics, Inc.. The 510(k) number is K921950.

When did SURGICAL DYNAMICS DISCOGRAPHY SYSTEM receive FDA 510(k) clearance?

SURGICAL DYNAMICS DISCOGRAPHY SYSTEM received FDA 510(k) clearance on 1993-06-07, under 510(k) number K921950.

Who is the listed applicant for SURGICAL DYNAMICS DISCOGRAPHY SYSTEM?

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

What is the FDA product code for SURGICAL DYNAMICS DISCOGRAPHY SYSTEM?

The FDA product code for SURGICAL DYNAMICS DISCOGRAPHY SYSTEM is FMI.

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Other records listing Surgical Dynamics, Inc. as applicant

K960046SURGICAL DYNAMICS 30K WORKING CHANNEL SCOPE K942987NUCLEOTOME L KIT K954193SURGICAL DYNAMICS 30K WORKING CHANNEL SCOPE & INSTRUMENT SET K950495SUGICAL DYNAMICS ENDOSCOPY IRRIGATION PUMP, CATALOG #3-4000 K931109NUCLEOTOME E KIT K923525NUCLEOTOME 3.5 MM AUTOMATED PERCUTANEOUS LUMBAR

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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.