510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K913730Substantially Equivalent

Aesculap Titanium Bone Plates

Aesculap Inc, South San Francisco CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913730 is the FDA 510(k) clearance record for AESCULAP TITANIUM BONE PLATES, a class II device, cleared for Aesculap, Inc. on under FDA product code KWQ (Appliance, Fixation, Spinal Intervertebral Body). FDA records list 269 510(k) clearances for Aesculap, Inc., from to . As of , FDA records show no recalls naming K913730.

Clearance record

Decision date
Received
(205 days to decision)
Product code
KWQ Appliance, Fixation, Spinal Intervertebral Body
Regulation
21 CFR 888.3060
Device class
Class II
Review panel
Orthopedic
Applicant
Aesculap, Inc. 1000 Gateway Blvd., South San Francisco CA
510(k) summary
Statement
Third party review
No

Clearances, product code KWQ

Trailing 12 months
11 clearances under product code KWQ in the twelve months to November 2026, March 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code KWQ, trailing twelve months
MonthClearances
December 20251
January 20260
February 20262
March 20263
April 20261
May 20262
June 20260
July 20261
August 20260
September 20261
October 20260
November 20260