Atlas FDA

STRYKER CEMENT REMOVAL SYSTEM

FDA 510(k) clearance K961101 · decided 1996-07-15

Clearance details

K-number
K961101
Device name
STRYKER CEMENT REMOVAL SYSTEM
Applicant
Stryker Corp.
Decision
Substantially Equivalent
Date received
1996-03-19
Decision date
1996-07-15
Days to decision
118 days
Clearance type
Traditional
Product code
LZV
Device class
2
Regulation number
888.4580
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Kalamazoo, MI, 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
OSCAR, MODEL OE3000 (K021502)Orthosonics, Ltd.2002-06-06
ACRYL-X II SYSTEM (K930629)Sonokinetics, Inc.1994-01-21
ORIGIN(TM) CEMENT EXTRACT SYST STD-PR/SPL-PR KITS (K904156)Origin Medsystems, Inc.1990-11-27
PROSTHETIC CEMENT REMOVER (K904180)Origin Medsystems, Inc.1990-11-20
IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR (K891472)Implant Technology, Inc.1989-05-02
PROSTHETIC CEMENT REMOVER (K890285)Albert K. Chin1989-04-19

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
VITAGEL RT3 SUTGICAL HEMOSTAT (P050044/S033)Stryker Corp.2017-03-02
VITAGEL RT3 SURGICAL HEMOSTAT (P050044/S032)Stryker Corp.2015-07-16
VITAGEL SURGICAL HEMOSTAT (RT3) (P050044/S031)Stryker Corp.2015-04-14
VITAGEL SURGICAL HEMOSTAT (RT3) (P050044/S030)Stryker Corp.2015-04-13
VITAGEL RT3 SURGICAL HEMOSTAT (P050044/S029)Stryker Corp.2014-12-12
VITAGEL RT3 DELIVERY SYSTEM (P050044/S028)Stryker Corp.2014-06-05
VITAGEL SURGICAL HEMOSTAT (VITAGEL) (P050044/S026)Stryker Corp.2014-02-11
RT3 SURGICAL HEMOSTAT (P050044/S027)Stryker Corp.2014-01-27