Surgicraft Lockdown Acromioclavicular (Ac) Device

FDA 510(k) K091207 · Surgicraft , Ltd.

Substantially Equivalent

510(k) numberK091207

Submission

Device name
Surgicraft Lockdown Acromioclavicular (Ac) Device
Applicant
Surgicraft , Ltd.
Douglassville, PA, US
Received
April 24, 2009
Decision date
February 15, 2011
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HTN – Washer, Bolt Nut
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was Surgicraft Lockdown Acromioclavicular (Ac) Device cleared by the FDA?

Surgicraft Lockdown Acromioclavicular (Ac) Device (K091207) received a 510(k) decision of Substantially Equivalent on February 15, 2011, 662 days after the submission was received.

What is the product code of K091207?

The FDA product code is HTN – Washer, Bolt Nut, a Class II (moderate risk) device regulated under 21 CFR 888.3030.