510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K070694Substantially Equivalent

Ccro (Craniocephalic Custom Remolding Orthosis)

Mike Miner, Kaysville UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K070694 is the FDA 510(k) clearance record for CCRO (CRANIOCEPHALIC CUSTOM REMOLDING ORTHOSIS), a class II device, cleared for Mike Miner on under FDA product code MVA (Orthosis, Cranial). FDA records list one 510(k) clearance for Mike Miner. As of , FDA records show no recalls naming K070694.

Clearance record

Decision date
Received
(181 days to decision)
Product code
MVA Orthosis, Cranial
Regulation
21 CFR 882.5970
Device class
Class II
Review panel
Neurology
Applicant
Mike Miner 1098 E. Mutton Hollow, Kaysville UT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MVA

Trailing 12 months

FDA records hold no clearances under product code MVA in the trailing twelve months.

FDA records show no clearances under product code MVA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MVA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260