Atlas FDA

RUSH PIN

FDA 510(k) clearance K903261 · decided 1990-07-30

Clearance details

K-number
K903261
Device name
RUSH PIN
Applicant
Onyx Medical Corp.
Decision
Substantially Equivalent
Date received
1990-07-24
Decision date
1990-07-30
Days to decision
6 days
Clearance type
Traditional
Product code
JDW
Device class
2
Regulation number
888.3040
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Memphis, TN, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
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XT3 System (K241357)Biodynamik, Inc.2025-01-22
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MAVERICK External Fixation System (K213874)Smith & Nephew, Inc.2022-02-11
Steinmann Pins and Kirschner Wires (K211508)Stryker GmbH2021-10-05
Extended HA Half Pins (K210784)Smith & Nephew, Inc.2021-04-02
Syntec Non-Sterile Steinmann Pins System (K200933)Syntec Scientific Corporation2020-05-05
Orthopedic Fixation Pin (K191803)Tinavi (Anhui) Medical Technologies Co., Ltd.2020-04-14
Temporary Fixation Pins (K192768)Eisertech, LLC2019-12-26
SMV Scientific K-Wire and Pins (K182171)Summit Medventures2018-10-25
Ultima HA Coated Half Pins and Wire (K163487)Vilex IN Tennessee, Inc.2017-02-13

Recalls involving this device

No recalls on record reference this clearance.