Blackstone Ascent Poct System Hooks (System Modification)

FDA 510(k) K033980 · Blackstone Medical, Inc.

Substantially Equivalent

510(k) numberK033980

Submission

Device name
Blackstone Ascent Poct System Hooks (System Modification)
Applicant
Blackstone Medical, Inc.
Springfield, MA, US
Received
December 23, 2003
Decision date
March 3, 2004
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KWP – Appliance, Fixation, Spinal Interlaminal
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3050
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was Blackstone Ascent Poct System Hooks (System Modification) cleared by the FDA?

Blackstone Ascent Poct System Hooks (System Modification) (K033980) received a 510(k) decision of Substantially Equivalent on March 3, 2004, 71 days after the submission was received.

What is the product code of K033980?

The FDA product code is KWP – Appliance, Fixation, Spinal Interlaminal, a Class II (moderate risk) device regulated under 21 CFR 888.3050.