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FDA 510(k)

Precision Thin Reciprocating Blade, 0.010in.

K-Number: K161514 · 2017-01-17

ApplicantStryker Corporation
Decision Date2017-01-17
Product CodeEQJ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

Precision Thin Reciprocating Blade, 0.010in. is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corporation. It received FDA 510(k) clearance on 2017-01-17 under 510(k) number K161514. The device is classified under product code EQJ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Precision Thin Reciprocating Blade, 0.010in.?

Precision Thin Reciprocating Blade, 0.010in. is a medical device that received FDA 510(k) clearance on 2017-01-17. The listed applicant is Stryker Corporation. The 510(k) number is K161514.

When did Precision Thin Reciprocating Blade, 0.010in. receive FDA 510(k) clearance?

Precision Thin Reciprocating Blade, 0.010in. received FDA 510(k) clearance on 2017-01-17, under 510(k) number K161514.

Who is the listed applicant for Precision Thin Reciprocating Blade, 0.010in.?

The FDA 510(k) record lists Stryker Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Precision Thin Reciprocating Blade, 0.010in.?

The FDA product code for Precision Thin Reciprocating Blade, 0.010in. is EQJ.

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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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