510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K994022Substantially Equivalent

Parallax Cranioset

Parallax Medical, Inc., Mountain View CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K994022 is the FDA 510(k) clearance record for PARALLAX CRANIOSET, a class II device, cleared for Parallax Medical, Inc. on under FDA product code GXP (Methyl Methacrylate For Cranioplasty). FDA records list 6 510(k) clearances for Parallax Medical, Inc., from to . As of , FDA records show no recalls naming K994022.

Clearance record

Decision date
Received
(279 days to decision)
Product code
GXP Methyl Methacrylate For Cranioplasty
Regulation
21 CFR 882.5300
Device class
Class II
Review panel
Neurology
Applicant
Parallax Medical, Inc. 453 Ravendale Dr., Suite B, Mountain View CA
510(k) summary
Summary
Third party review
No

Clearances, product code GXP

Trailing 12 months
4 clearances under product code GXP in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GXP, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20261
April 20260
May 20260
June 20261
July 20261
August 20260
September 20260
October 20260