Medline ReNewal Reprocessed Harmonic FOCUS+ Shears without Adaptive Tissue Technology

FDA 510(k) K150524 · Surgical Instrument Services and Savings, Inc.

Substantially Equivalent

510(k) numberK150524

Submission

Device name
Medline ReNewal Reprocessed Harmonic FOCUS+ Shears without Adaptive Tissue Technology
Applicant
Surgical Instrument Services and Savings, Inc.
Redmond, OR, US
Received
March 2, 2015
Decision date
December 16, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NLQ – Single-Use Reprocessed Ultrasonic Surgical Instruments
Device class
Unclassified

Single-use reprocessed versions of the ultrasonic devices used in surgical procedures either for fragmentation, emulsification and aspiration of soft tissue and hard tissue or for ligation of vessels (under product code “LFL”). Reprocessing validation data for this device type must be included in a 510(k) submission.. (70 FR 56911, available at…

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More from Stryker Sustainability Solutions

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Questions and answers

When was Medline ReNewal Reprocessed Harmonic FOCUS+ Shears without Adaptive Tissue Technology cleared by the FDA?

Medline ReNewal Reprocessed Harmonic FOCUS+ Shears without Adaptive Tissue Technology (K150524) received a 510(k) decision of Substantially Equivalent on December 16, 2015, 289 days after the submission was received.

What is the product code of K150524?

The FDA product code is NLQ – Single-Use Reprocessed Ultrasonic Surgical Instruments, a Unclassified device.