Atlas FDA

TITANIUM CLASSIC COMPRESSION HIP SCREW SYSTEM

FDA 510(k) clearance K952697 · decided 1995-09-12

Clearance details

K-number
K952697
Device name
TITANIUM CLASSIC COMPRESSION HIP SCREW SYSTEM
Applicant
Smith & Nephew Richards, Inc.
Decision
Substantially Equivalent
Date received
1995-06-13
Decision date
1995-09-12
Days to decision
91 days
Clearance type
Traditional
Product code
HWC
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.

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TriMed Compression Screws (K261241)TriMed, Inc.2026-05-14
Arthrex Beaming System (K254215)Arthrex, Inc.2026-05-08
OSSIOfiber® Threaded Trimmable Fixation Nail (K254077)OSSIO , Ltd.2026-05-01
TITAN Nail; APTUS K-Wire System (K260934)Medartis AG2026-04-17
CoAptix S System (K252699)University of Utah, Department of Orthopaedics2026-04-10
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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
OSTEOPAL (P810020/S005)Smith & Nephew Richards, Inc.1998-10-15
PALACOS E-FLOW (OSTEOPAL) BONE CEMENT (P810020/S004)Smith & Nephew Richards, Inc.1998-07-30
PALACOS R BONE CEMENT (P810020/S003)Smith & Nephew Richards, Inc.1992-02-14
PALACOS R BONE CEMENT (P810020/S002)Smith & Nephew Richards, Inc.1989-01-30
PALACOS R BONE CEMENT (P810020/S001)Smith & Nephew Richards, Inc.1984-08-14
PALACOS R BONE CEMENT (P810020)Smith & Nephew Richards, Inc.1984-02-02