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 a medical device manufactured by Stryker Corporation. It received FDA 510(k) clearance on 2017-01-17 under approval 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. It is manufactured by Stryker Corporation. The 510(k) number is K161514.
When was Precision Thin Reciprocating Blade, 0.010in. approved by the FDA?
Precision Thin Reciprocating Blade, 0.010in. received FDA 510(k) clearance on 2017-01-17, under approval number K161514.
What company makes Precision Thin Reciprocating Blade, 0.010in.?
Precision Thin Reciprocating Blade, 0.010in. is manufactured by Stryker Corporation.
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.
Other Devices by Stryker Corporation
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.