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FDA 510(k)

DVR® Crosslock Wrist Spanning Plate (131849181)

K-Number: K220244 · 2022-04-28

ApplicantPioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech
Decision Date2022-04-28
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DVR® Crosslock Wrist Spanning Plate (131849181) is a medical device manufactured by Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech. It received FDA 510(k) clearance on 2022-04-28 under approval number K220244. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DVR® Crosslock Wrist Spanning Plate (131849181)?

DVR® Crosslock Wrist Spanning Plate (131849181) is a medical device that received FDA 510(k) clearance on 2022-04-28. It is manufactured by Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech. The 510(k) number is K220244.

When was DVR® Crosslock Wrist Spanning Plate (131849181) approved by the FDA?

DVR® Crosslock Wrist Spanning Plate (131849181) received FDA 510(k) clearance on 2022-04-28, under approval number K220244.

What company makes DVR® Crosslock Wrist Spanning Plate (131849181)?

DVR® Crosslock Wrist Spanning Plate (131849181) is manufactured by Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech.

What is the FDA product code for DVR® Crosslock Wrist Spanning Plate (131849181)?

The FDA product code for DVR® Crosslock Wrist Spanning Plate (131849181) is HRS.

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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.

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