Osteonics Restoration Monolithic II Slotted Hip Stem Series

FDA 510(k) K951671 · Osteonics Corp.

Substantially Equivalent

510(k) numberK951671

Submission

Device name
Osteonics Restoration Monolithic II Slotted Hip Stem Series
Applicant
Osteonics Corp.
Allendale, NJ, US
Received
April 11, 1995
Decision date
September 6, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MEH – Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3353
Specialty
Orthopedic
Implant
Yes

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K984302Osteonics Spinal System Cylindrical Bone ScrewsMNH · Special 12/18/1998SE
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Questions and answers

When was Osteonics Restoration Monolithic II Slotted Hip Stem Series cleared by the FDA?

Osteonics Restoration Monolithic II Slotted Hip Stem Series (K951671) received a 510(k) decision of Substantially Equivalent on September 6, 1995, 148 days after the submission was received.

What is the product code of K951671?

The FDA product code is MEH – Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate, a Class II (moderate risk) device regulated under 21 CFR 888.3353.