CRW®

Universal Compact Head Ring Crossbar Attachment Screw

Registry build 21.09.26
5manufacturers in China registered for this device type
107catalogue numbers in this listing
1510(k) clearance
4recalls on this code

Who Else Makes It

Concentrated in Jiangsu (2), Shanghai (1), Shandong (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HAW
Manufacturer City Province Registered as Device types
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Sinovation (Beijing) Medical Technology Co., Ltd. Beijing Beijing Manufacturer 1

Record

Regulatory record for CRW®
Listed by Integra Lifesciences Corporation, United States
FDA product code HAW
Device type Neurological Stereotaxic Instrument
Device class Class 2
Regulation 21 CFR 882.4560
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K160811
Record published 2017-04-14
Record revised 2025-11-07 (version 8)

Specifications

Specifications
MRI safety MR Conditional
Sterilisation Ethylene Oxide
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date, serial number
Packaging Pouch of 5
Distribution end date 2023-12-04
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for CRW®
Catalogue number Size Per pack Status
S2021170402 In distribution
CTCPTO In distribution
DADS27 In distribution
DHRSL5 10 In distribution
DHRSS5 10 In distribution
CRWASP In distribution
UCHR In distribution
DADS32 In distribution
DA63GB In distribution
CSS In distribution
CRWFASP In distribution
SHDWHS0816OC In distribution
DS25 In distribution
SD46 In distribution
ASD1 In distribution
S2021170401 In distribution
CSSI In distribution
UCHRCBS In distribution
DS30 In distribution
DADS63 In distribution
DADS46 In distribution
DHRSS5 10 In distribution
NBND5 In distribution
HRDXS In distribution
CRWMA In distribution
S72350450 In distribution
SHDWKN0023 In distribution
CRWPBSHK In distribution
SDD In distribution
CTCPGEMF In distribution
DA63 In distribution
RT20160 In distribution
DS16 1.6 mm In distribution
DA63GS In distribution
S2021170403 In distribution
DS20 In distribution
DS21 In distribution
CTCPS In distribution
CRWPBS In distribution
S2021170405 In distribution
SDK In distribution
CRWTBSS In distribution
DHRSL5 10 In distribution
NBND In distribution
HRIMTSC In distribution
UCHRP In distribution
CRWFMA In distribution
UCHREB In distribution
CTCPP2 In distribution
CRWBP In distribution
HRAIM In distribution
HREBA In distribution
UCHRCB1 Withdrawn
CRWPMDB25 Withdrawn
CCO Withdrawn
S72901056 Withdrawn
RT25116 Withdrawn
CRWASL Withdrawn
RT0776 Withdrawn
DS18 Withdrawn
HRIMS Withdrawn
CRWPMDD Withdrawn
CRWHK Withdrawn
CRWASGB Withdrawn
CTVC Withdrawn
CTCPGP Withdrawn
CRWPBSRAID Withdrawn
RB Withdrawn
GSKCN20 Withdrawn
GSKSS30210 Withdrawn
BRWASPW Withdrawn
CTCPP Withdrawn
OTDRFNI Withdrawn
RB20 Withdrawn
ST1002 Withdrawn
GSKSS20 Withdrawn
CRWMCPH30 Withdrawn
CRWPMDB16 Withdrawn
S72901984 Withdrawn
CRWPMDB20 Withdrawn
RT2576 Withdrawn
CRWRAID Withdrawn
ATLASSW Withdrawn
CRWAPBS Withdrawn
CRWP30 Withdrawn
IF3000 Withdrawn
RT07116 Withdrawn
CDEKGS Withdrawn
CSL Withdrawn
GSKSS25220 Withdrawn
GSKCN30210 Withdrawn
SCSWCD Withdrawn
DA63D Withdrawn
CRWPRECISE Withdrawn
BRWLF Withdrawn
CTCPE Withdrawn
S72901055 Withdrawn
HRKTP Withdrawn
CRWPMDB30 Withdrawn
MRCTF2 100 Withdrawn
S72901978 Withdrawn
CRWMS Withdrawn
GSKCN25220 Withdrawn
CTCPGE9800 Withdrawn
RLPP Withdrawn
LATLSKB Withdrawn
CRWCASE Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Neurological Stereotaxic Instrument Medtronic Navigation, Inc. 844
PMT Corporation – Stereotactic PMT Corp. 255
Leksell Stereotactic System Elekta Instrument AB 199
Neurological Stereotaxic Instrument Inomed Medizintechnik Gmbh 146
Neurological Stereotaxic Instrument Stryker Leibinger Gmbh & Co. KG 125
Geniant Cranial KOH Young Technology Inc. 113
Leksell Stereotactic System Elekta Solutions AB 93
microTargeting™ Insertion Tube with Stylet FHC, Inc. 60
Leksell Stereotactic System Neurosurgical Instruments Elekta Instrument AB 58
Leksell Vantage Stereotactic System Elekta Instrument AB 53
Stealth Autoguide™ System Medtronic Navigation, Inc. 50
microTargeting™ Insertion Tube FHC, Inc. 48

Showing 12 of 1,137. All products under Neurological Stereotaxic Instrument

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K160811 2016-12-06

Recalls Naming This Product

4 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of CRW®
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Integra Lifesciences Corporation 510(k) number 2015-08-21 Class II Process design Integra identified that the UCHRAP component (Arc Adapter Plate) would not assemble properly to the UCHRAR component (ARC Adapter Ring) of the Compact Head Ring Adapter due to an error in the manufacturing drawing. 6 units 2016-10-13
Integra Lifesciences Corporation 510(k) number 2012-08-09 Class II Device Design T-handle screw is used on a complementary product to the CRW, the Integra HRAIM, which is the CT-compatible intubation Head Ring Assembly. When the T-handle on the HRAIM intubation hoop is tightened, the T-handle could stop in a vertical p 175 units 2014-03-26
Integra Lifesciences Corporation 510(k) number 2012-08-09 Class II Device Design T-handle screw is used on a complementary product to the CRW, the Integra HRAIM, which is the CT-compatible intubation Head Ring Assembly. When the T-handle on the HRAIM intubation hoop is tightened, the T-handle could stop in a vertical p 188 units 2014-03-26
Integra Lifesciences Corporation 510(k) number 2011-01-12 Not classified Manufacturing material removal Overall length of the intubation hoop in the HRAIM Intubation Head Ring Assembly is too long and will not allow a device to to attach 8 units 2011-04-04

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer