510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930319Substantially Equivalent

Osteon Adaptor/cradle

United American Medical Co., Inc., Mc Minnville TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930319 is the FDA 510(k) clearance record for OSTEON ADAPTOR/CRADLE, a class I device, cleared for United American Medical Co., Inc. on under FDA product code HWE (Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment). FDA records list 3 510(k) clearances for United American Medical Co., Inc., from to . As of , FDA records show no recalls naming K930319.

Clearance record

Decision date
Received
(350 days to decision)
Product code
HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
Regulation
21 CFR 878.4820
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
United American Medical Co., Inc. 216 E. Main St., Mc Minnville TN
510(k) summary
Statement
Third party review
No

Clearances, product code HWE

Trailing 12 months

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

FDA records show no clearances under product code HWE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HWE, 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