Ring Upm Total Hip Replacement

FDA 510(k) K864515 · Downs Surgical , Ltd.

Substantially Equivalent

510(k) numberK864515

Submission

Device name
Ring Upm Total Hip Replacement
Applicant
Downs Surgical , Ltd.
Mitcham Surrey, GB
Received
November 17, 1986
Decision date
March 13, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KWA – Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)
Device class
Class III (high risk)
Regulation
21 CFR 888.3330
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was Ring Upm Total Hip Replacement cleared by the FDA?

Ring Upm Total Hip Replacement (K864515) received a 510(k) decision of Substantially Equivalent on March 13, 1987, 116 days after the submission was received.

What is the product code of K864515?

The FDA product code is KWA – Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component), a Class III (high risk) device regulated under 21 CFR 888.3330.